RESUMO
BACKGROUND: Autosomal recessive ichthyosis leads to structural or biochemical changes that impair skin barrier function. HYPOTHESIS/OBJECTIVES: To assess (1) the phenotype and genotype in a litter of Jack Russell Terriers with autosomal recessive congenital ichthyosis (ARCI), and (2) the defective skin barrier and determine if a topical ceramide can modulate the barrier. ANIMALS: A healthy dam and litter of Jack Russell Terrier puppies (healthy male, affected male and female), one affected adult Jack Russell Terrier and one unrelated healthy Jack Russell Terrier. MATERIALS AND METHODS: A severe cornification defect was identified via examination of affected puppies. As the phenotype worsened, the affected puppies received a topical application of ω-0-acylceramide for 10 days. Before humane euthanasia, the skin barrier was evaluated via transepidermal water loss (TEWL), corneometry and pH in affected dogs. Genomic testing was performed, and skin samples were analysed by light and electron microscopy. RESULTS: Affected puppies were homozygous for the 1980 bp LINE-1 insertion in the TGM1 (transglutaminase 1) gene; the unaffected littermate and the dam were heterozygous carriers. ARCI puppies were underweight and had a severe hyperkeratotic phenotype that impaired mobility. TEWL was markedly higher in affected dogs. The cutaneous pH of affected puppies was higher than the normal littermate. Treatment of the skin with ω-0-acylceramide normalised the pH to match the littermate and decreased TEWL. Electron microscopy revealed marked attenuation of the cornified envelope. CONCLUSIONS AND CLINICAL RELEVANCE: Dogs with TGM1-deficient ARCI have an impaired skin barrier. Topical therapy can partially repair the barrier defect.
RESUMO
Darier disease is caused by heterozygous loss of function variants in the ATP2A2 gene encoding the endoplasmic/sarcoplasmic reticulum Ca2+ pump ATP2A2. Defective intracellular calcium signaling in the epidermis results in a loss of desmosomal adhesion and the development of characteristic skin lesions. In this study, we investigated a Shih Tzu that developed erythematous papules on the ventrum and, over time, the dorsal neck and a nodule in the right ear canal with secondary ear infection. Histopathologic examination demonstrated discrete foci of acantholysis affecting suprabasal layers of the epidermis. Whole genome sequencing of the affected dog identified a heterozygous missense variant, p.N809H, affecting an evolutionarily conserved amino acid residue of the ATP2A2 protein. The highly characteristic clinical and histopathologic findings together with a plausible variant in the only known functional candidate gene establish the diagnosis of canine Darier disease in the studied dog and highlight the potential of genetic analyses as complementary diagnostic approach in veterinary medicine.
Assuntos
Doença de Darier , Doenças do Cão , Animais , Cães , Doença de Darier/genética , Doença de Darier/veterinária , Doença de Darier/diagnóstico , Mutação de Sentido Incorreto , Heterozigoto , Cálcio/metabolismo , Linhagem , Doenças do Cão/genéticaRESUMO
Cutaneous mastocytosis (CM) is a rare condition in young dogs characterized by multicentric cutaneous proliferation of neoplastic mast cells. Clinical data from 8 dogs that met inclusion criteria (age of onset less than 1.5 years, greater than 3 lesions) were obtained via a standardized survey. Biopsy samples were classified by the Kiupel/Patnaik grading systems and analyzed for c-KIT mutations. The median age of onset was 6 months (range: 2-17 months). Dogs had 5 to more than 50 lesions characterized as nodules, plaques, and papules. Seven dogs were pruritic. Clinical staging in 2 dogs did not reveal visceral involvement. No dogs had systemic illnesses at diagnosis. Histologically, CM was similar to cutaneous mast cell tumor (cMCT). Two dogs had neoplasms classified as high-grade/grade II while 6 dogs had low-grade/grade II neoplasms. No dogs had mutations in c-KIT exons 8 and 11. Treatment included antihistamines (8/8), corticosteroids (7/8), lokivetmab (3/8), and toceranib (1/8). Six dogs were alive with lesions at the end of the study with a median follow-up time of 898 days, while 2 dogs were euthanized. In dogs with high-grade/grade II neoplasms, one continued to develop lesions at 1922 days post-diagnosis, while the other dog was euthanized at 56 days post-diagnosis. One dog was euthanized 621 days post-diagnosis due to rupture of a neoplasm. CM occurs in young dogs and is histologically indistinguishable from cMCT. Current histologic grading systems did not apply uniformly to the dogs of the study and further studies are needed.
Assuntos
Doenças do Cão , Mastocitose Cutânea , Neoplasias Cutâneas , Cães , Animais , Mastocitose Cutânea/diagnóstico , Mastocitose Cutânea/veterinária , Mastocitose Cutânea/patologia , Pele/patologia , Neoplasias Cutâneas/diagnóstico , Neoplasias Cutâneas/veterinária , Neoplasias Cutâneas/patologia , CME-Carbodi-Imida , Doenças do Cão/diagnóstico , Doenças do Cão/patologia , Mastócitos/patologiaRESUMO
Allergic dermatoses are common in people and domestic animals. Resultant lesions are routinely biopsied and submitted for histological examination to confirm a diagnosis or rule out diseases with overlapping or atypical clinical features. Diagnostic pathologists and clinicians are often faced with the difficult task of determining whether an allergic reaction pattern is present on both the microscopic and macroscopic levels and correlating histopathologic findings with clinical and historical data to achieve a precise clinical diagnosis. The bulk of the current veterinary literature on allergic dermatoses focuses on atopic dermatitis in dogs, distantly followed by cats, horses, and other animals. The objectives of this review are to demonstrate the key histopathologic and clinical diagnostic features of the various allergy-mediated reaction patterns, and to provide diagnosticians with a practical guide for clinicopathological correlations. Current concepts in the pathophysiology of immediate hypersensitivity reactions, with a focus on atopic dermatitis, are discussed. Points of potential histopathologic overlap between the "classic" allergic reaction pattern and less common inflammatory, predominately eosinophilic, conditions that may mimic this pattern will be discussed with the goal of highlighting the critical need for collaboration between pathologists and clinicians in furthering patient care.
Assuntos
Doenças do Gato , Dermatite Atópica , Doenças do Cão , Doenças dos Cavalos , Hipersensibilidade , Cães , Animais , Gatos , Cavalos , Dermatite Atópica/diagnóstico , Dermatite Atópica/veterinária , Hipersensibilidade/diagnóstico , Hipersensibilidade/veterinária , Biópsia/veterinária , Animais Domésticos , Doenças do Cão/diagnósticoRESUMO
Pattern analysis of inflammatory skin diseases is a technique that offers a systematic approach to the histologic diagnosis of skin diseases. First introduced to human dermatopathology in the 1970s, it was widely adopted by veterinary pathologists for the histologic diagnosis of skin diseases in animals. As the inflammatory pattern reflects, to varying extents, aspects of the underlying disease pathogenesis, its use has contributed to the recognition of novel skin diseases in domestic animals, particularly in dogs and cats. Alternative diagnostic approaches used in human dermatopathology, such as "tissue-reaction pattern" and a purely "anatomic approach" have not been as widely used in veterinary pathology. However, veterinary pathologists often combine pattern analysis with anatomic and etiologic factors. This overview outlines the technique, introduces the patterns, and discusses advantages and limitations of pattern analysis in veterinary diagnostic dermatopathology. While molecular analytic techniques and image informatics will undoubtedly prove to be revolutionary in many areas of diagnostic pathology, it is recognized in both human and veterinary arenas that the light microscopic interpretation of hematoxylin and eosin-stained tissue sections will remain the mainstay of routine dermatopathology diagnosis for the foreseeable future.
Assuntos
Doenças do Gato , Dermatite , Doenças do Cão , Dermatopatias , Humanos , Animais , Gatos , Cães , Doenças do Gato/diagnóstico , Doenças do Gato/patologia , Doenças do Cão/diagnóstico , Doenças do Cão/patologia , Dermatopatias/diagnóstico , Dermatopatias/veterinária , Dermatite/diagnóstico , Dermatite/veterinária , Dermatite/patologia , Microscopia/veterináriaRESUMO
German Shorthaired Pointer (GSHP) dogs with a UNC93B1 gene mutation develop exfoliative cutaneous lupus erythematosus (ECLE) and kidney disease resembling lupus nephritis in humans. The objective of this study was to characterize the kidney disease by light microscopy, immunofluorescence, and electron microscopy in a population of GSHP dogs with ECLE. Medical records were reviewed, and light microscopy of kidneys from 7 GSHP dogs with a previous histologic diagnosis of ECLE was performed. Immunofluorescence of fresh-frozen kidney from 1 dog and transmission electron microscopy of kidney from that dog and 2 additional dogs were performed. Five of 7 dogs had proteinuria diagnosed by urinalysis or urine protein-to-creatinine ratio. Two of 7 dogs were intermittently hypoalbuminemic, and none were azotemic. Histologic findings included early (2 dogs) to late (5 dogs) membranous glomerulonephropathy characterized by mild-to-severe glomerular capillary loop thickening and tubular proteinosis. In all 7 cases, trichrome staining revealed red granular immune deposits on the subepithelial surface of the glomerular basement membrane. Immunofluorescence revealed strong granular labeling for immunoglobulins and complement protein C3. Electron microscopy demonstrated subepithelial electron-dense immune deposits encircled by the remodeled glomerular basement membrane. These findings are diagnostic of immune-complex membranous glomerulonephropathy and are similar to class V lupus in humans. This cohort of GSHP dogs with ECLE developed immune-complex membranous glomerulonephropathy, which we hypothesize is a manifestation of systemic lupus erythematosus. GSHP dogs with ECLE should undergo clinical evaluation of renal function for early identification and treatment.
Assuntos
Doenças do Cão , Glomerulonefrite Membranosa , Nefropatias , Lúpus Eritematoso Cutâneo , Lúpus Eritematoso Sistêmico , Humanos , Cães , Animais , Glomerulonefrite Membranosa/diagnóstico , Glomerulonefrite Membranosa/veterinária , Glomerulonefrite Membranosa/patologia , Rim/patologia , Glomérulos Renais/patologia , Lúpus Eritematoso Cutâneo/tratamento farmacológico , Lúpus Eritematoso Cutâneo/genética , Lúpus Eritematoso Cutâneo/patologia , Lúpus Eritematoso Cutâneo/veterinária , Lúpus Eritematoso Sistêmico/patologia , Lúpus Eritematoso Sistêmico/veterinária , Nefropatias/patologia , Nefropatias/veterinária , Doenças do Cão/diagnóstico , Doenças do Cão/genéticaRESUMO
Canine cutaneous epitheliotropic T-cell lymphoma is a neoplasm with heterogeneous clinical and histopathological presentations. Survival times and responses to therapy are variable, and indicators to predict outcomes are lacking. Clinical and histopathological parameters from 176 archival cases from the University of Pennsylvania and University of Bern (2012-2018) were investigated for associations with clinical outcomes. Histopathological evaluation used digitized whole slide images and QuPath software. Cases included 107 female and 69 male dogs from 48 breeds, with a mean age of 10.4 years. Most common clinical signs were erythema (n = 131), crusting (n = 108), and scaling (n = 102). Affected sites were haired skin (n = 159), lip (n = 74), nasal planum (n = 49), and paw pads (n = 48). The median survival time (MST) was 95 days (1-850). Dogs had 4.26-fold and 2.82-fold longer MST when treated with chemotherapy and prednisone, respectively, than when receiving supportive care. Haired skin involvement (hazard ratio [HR]: 2.039, 95% confidence interval [CI]: 1.180-3.523), erosions/ulcers (HR: 1.871, 95% CI: 1.373-2.548), nodules (HR: 1.496, 95% CI: 1.056-2.118), and crusting (HR: 1.454, 95% CI: 1.061-1.994) were clinical parameters predicting poor outcomes, whereas complete posttherapeutic clinical remission (HR: 0.469, 95% CI: 0.324-0.680) and a stable disease (HR: 0.323, 95% CI: 0.229-0.456) were associated with longer survival. Histopathological features associated with the increased risk of death were extensive infiltration of the panniculus (HR: 2.865, 95% CI: 1.565-4.809), mitotic count ≥7/high-power field (HR: 3.027, 95% CI: 2.065-4.439), cell diameter ≥10.0 µm (HR: 2.078, 95% CI: 1.281-3.372), and nuclear diameter ≥8.3 µm (HR: 3.787, 95% CI: 1.647-8.707).
Assuntos
Doenças do Cão , Linfoma Cutâneo de Células T , Neoplasias Cutâneas , Masculino , Cães , Animais , Feminino , Prognóstico , Neoplasias Cutâneas/patologia , Neoplasias Cutâneas/veterinária , Pele/patologia , Linfoma Cutâneo de Células T/diagnóstico , Linfoma Cutâneo de Células T/veterinária , Doenças do Cão/patologiaRESUMO
BACKGROUND: Dermal arteritis of the nasal philtrum (DANP) has been described in large-breed dogs. OBJECTIVES: To characterise clinically distinct, discrete fissures of the dorsolateral nasal alae associated with severe bleeding in German shepherd dogs (GSDs). ANIMALS: Fourteen privately owned GSDs with linear rostrolateral nasal alar fissures and a histopathological diagnosis of nasal vasculopathy. MATERIALS AND METHODS: Retrospective analysis of medical records and histological slides. RESULTS: Mean age of onset was 6 years. Before biopsy, episodic arteriolar bleeding was noted in 11 of the 14 (79%) dogs. Slide analysis revealed enlarged nasal arterioles with expanded vascular tunics and luminal stenosis beneath ulcers. Histopathological lesions consistent with mucocutaneous pyoderma and/or facial discoid lupus erythematosus were present in 5 of the 14 (36%) dogs. Enlarged arterioles stained blue with Alcian blue and Masson's trichrome stains, consistent with deposition of mucin and collagen, respectively. Immunohistochemical stains (neutrophil myeloperoxidase, IBA1, CD3) were performed. CD3 was negative for all dogs, whilst neutrophil myeloperoxidase and IBA1 occasionally demonstrated intramural neutrophils (3 of the 14 dogs, 21%) or histiocytes (1 of the 14 dogs, 7%) in altered vessels, respectively. All dogs underwent medical management and/or surgical excision. Treatments included tacrolimus, prednisone, ciclosporin-modified, pentoxifylline, antimicrobials and doxycycline/niacinamide. No dogs were treated with antimicrobials alone. For seven dogs with long-term follow-up, treatment response was complete in five (71%) and partial in two (29%), with six of the seven (86%) receiving immunomodulatory treatments to maintain remission. CONCLUSION AND CLINICAL RELEVANCE: Nasal alar arteriopathy of GSDs shares histopathological changes with DANP. It has characteristic clinical and histopathological features and appears amenable to immunomodulation.
Assuntos
Arterite , Doenças do Cão , Pioderma , Cães , Animais , Estudos Retrospectivos , Peroxidase/uso terapêutico , Doxiciclina/uso terapêutico , Ciclosporina/uso terapêutico , Pioderma/veterinária , Arterite/diagnóstico , Arterite/veterinária , Doenças do Cão/tratamento farmacológicoRESUMO
Epidermolysis bullosa (EB) is a group of blistering disorders that includes several subtypes, classified according to their level of cleavage. Typical clinical signs are blisters and erosions resulting from minimal trauma. The disease has been described in many mammalian species and pathogenic variants in at least 18 different genes have been identified. In the present study, we investigated a Cardigan Welsh Corgi with congenital clinical signs consistent with epidermolysis bullosa. The puppy had blisters and erosions on the paw pads, and the oral mucosa. Histologic examination demonstrated the typical clefting between the dermis and epidermis and confirmed the clinical suspicion. We obtained whole genome sequencing data from the affected puppy and searched for variants in candidate genes known to cause EB. This revealed a heterozygous missense variant, KRT5:p.(E476K), affecting the highly conserved KLLEGE motif of keratin 5. The mutant allele in the affected puppy arose owing to a de novo mutation event as it was absent from both unaffected parents. Knowledge of the functional impact of KRT5 variants in other species together with the demonstration of the de novo mutation event establishes KRT5:p.(E476K) as causative variant for the observed EBS.
Assuntos
Doenças do Cão , Epidermólise Bolhosa Simples , Cães , Animais , Epidermólise Bolhosa Simples/genética , Epidermólise Bolhosa Simples/patologia , Queratina-5/genética , Queratina-14/genética , Vesícula , Mutação de Sentido Incorreto , MamíferosRESUMO
Palisading granulomatous dermatitis and panniculitis is recognized in various cutaneous inflammatory lesions secondary to presumed collagen damage. Cutaneous nodules with a palisading arrangement of histiocytes surrounding foci of collagen degeneration have been clinically termed palisading granuloma in dogs. Study aims were to characterize the cellular infiltrate of canine palisading granuloma and document salient clinical features. Inclusion criteria were met for 36 dogs and encompassed nodular dermal and subcutaneous histiocyte-predominant cellular infiltrates targeting and enveloping collagen fibers/necrotic foci with palisading configurations. Infectious causes were ruled out via standard histochemical stains and/or clinical data. Medical records were reviewed for signalment, clinical features, treatment, outcome, and comorbidities. Immunohistochemistry (IBA1, CD204, E-cadherin) and Masson's trichrome stain were used to assess histiocytic populations and dermal collagen, respectively. The histiocytes had moderate or strong immunolabeling for IBA1 and CD204 in 36/36 dogs (100%) and mild positive immunolabeling for E-cadherin in 3/36 dogs (8%). Alteration of collagen was graded as moderate or strong in 32/36 dogs (89%) and mild in 3/36 dogs (8%). Large breeds predominated with 30/36 dogs (83%) being ≥23 kg. Focal nodules were identified in 31/36 dogs (86%). The head/face were involved in 19/36 dogs (53%) and the extremities in 18/36 dogs (50%). Lesions from the 5/36 dogs (14%) with multiple nodules contained prominent eosinophilic infiltrates. Following excision, there was no evidence of recurrence. In conclusion, palisading granulomas are a distinct, non-neoplastic, histiocyte-predominant inflammatory condition in dogs associated with altered dermal collagen and favorable prognosis.
Assuntos
Doenças Autoimunes , Dermatite , Doenças do Cão , Paniculite , Animais , Doenças Autoimunes/veterinária , Dermatite/veterinária , Cães , Granuloma/veterinária , Histiócitos , Paniculite/veterináriaRESUMO
The stratum corneum (SC), the outermost layer of the epidermis, serves a crucial role in maintaining body hydration and protection from environmental insults. When the stratum corneum is injured or when the genetic blueprints are flawed, the body is at risk of dehydration, secondary infections and allergen sensitization. Advancements in veterinary dermatology have revealed a wide gamut of disease from relatively benign to lethal that specifically arise from flawed structural proteins, enzymes or lipids needed to create the corneocytes and lipid bilayers of the SC. Some conditions closely mimic their human counterparts while others are unique to the dog. This review will focus on forms of ichthyosis in the dog.
La cornéogénèse est le processus par lequel les kératinocytes subissent une différenciation terminale de la couche basale de l'épiderme à la couche cornée hautement spécialisée (SC). Les termes cornéogénèse et kératinisation sont souvent utilisés comme synonymes ; la différence résulte de leur dérivation grecque (keras) versus latine (cornu). Les cornéocytes entièrement différenciés finissent par se répandre dans l'environnement sous forme de squame. En microscopie optique avec coloration de routine, les couches les plus externes de l'épiderme apparaissent sous la forme de minces disques éosinophiles entrelacés (arrangement dit "en tissage") qui est un artefact créé par la perte de lipides intercellulaires pendant le traitement des tissus (Figure 1). Bien qu'historiquement ignorés en tant que débris tissulaires, le SC est maintenant connu pour être indispensable à la fois pour maintenir l'hydratation du corps et pour se protéger des agressions environnementales. En effet, l'acquisition du SC hydrophobe était une réalisation évolutive majeure qui a permis la colonisation terrestre des terres par des mammifères aquatiques intrépides. Il convient de noter que nos connaissances actuelles sur la fonction de barrière cutanée et le processus de cornéogénèse reposent en grande partie sur des études sur des souris sans poils, immunocompétentes (c'est-à-dire Skh1) et sur la peau humaine. Cependant, nos chiens de compagnie peuvent également fournir de nombreuses informations. Les modèles murins d'ingénierie (par exemple, les knock-out Pnlp1 et Nipal4) d'ichtyose congénitale autosomique récessive (ARCI) sont généralement mortels à la naissance, tandis que les chiens avec un ARCI comparable vivent en bonne santé malgré une mise à l'échelle excessive. Il est bien établi que certaines maladies spontanées chez le chien (par exemple, la dermatite atopique) imitent davantage les conditions humaines que les modèles murins induits chimiquement ou génétiquement. Cette revue se concentre sur ces troubles chez le chien et, le cas échéant, les conditions comparables chez l'homme.
La cornificación es el proceso mediante el cual los queratinocitos experimentan una diferenciación terminal desde la capa basal de la epidermis hasta el estrato córneo (SC) altamente especializado. Los términos cornificación y queratinización se utilizan a menudo como sinónimos; la diferencia resulta de su derivación griega (keras) versus latina (cornu). Los corneocitos completamente diferenciados eventualmente se desprenden al medio ambiente como escamas. En la microscopía óptica con tinción de rutina, las capas más externas de la epidermis aparecen como discos entrelazados eosinófilos delgados (la denominada disposición de "tejido en cesta"), que es un artefacto creado por la pérdida de lípidos intercelulares durante el procesamiento del tejido (Figura 1). Si bien históricamente se ha ignorado como restos de tejido, ahora se sabe que el SC es indispensable tanto para mantener la hidratación corporal como para protegerlo de las agresiones ambientales. De hecho, la obtención del SC hidrofóbico fue un logro evolutivo importante que permitió la colonización terrestre de la tierra por intrépidos mamíferos acuáticos. Cabe señalar que nuestro conocimiento actual de la función de la barrera cutánea y el proceso de cornificación se basa en gran medida en estudios en ratones inmunocompetentes sin pelo (es decir, Skh1) y piel humana; sin embargo, nuestros perros de compañía también pueden proporcionar información abundante.2 Los modelos de ratón genéticamente seleccionados (p. ej., knockouts de Pnlp1 y Nipal4) con ictiosis congénita autosómica recesiva (ARCI) suelen ser letales al nacer, mientras que los perros con ARCI comparables viven vidas saludables a pesar de la descamación excesiva. 4 Está bien establecido que algunas enfermedades espontáneas en los perros (por ejemplo, la enfermedad atópica de la piel) imitan las condiciones humanas más que los modelos de ratón inducidos química o genéticamente.5 Esta revisión se centra en estos trastornos en los perros y, en momentos apropiados, en los condiciones comparables en humanos.
Cornificação é o processo pelo qual os queratinócitos sofrem diferenciação terminal desde a camada basal da epiderme até o altamente especializado estrato córneo (SC). Os termos cornificação e queratinização são frequentemente usados como sinônimos; a diferença resulta de sua derivação grega (keras) versus latina (cornu). Os corneócitos totalmente diferenciados são eventualmente eliminados no ambiente na forma de escamas. À microscopia ótica com corantes de rotina, as camadas mais externas da epiderme aparecem como discos eosinofílicos entrelaçados finos (o chamado arranjo em bolsa de cesto), que é um artefato criado pela perda de lipídios intercelulares durante o processamento do tecido (Figura 1). Embora historicamente tenha sido considerado como debris teciduais, o SC agora é conhecido por ser indispensável tanto para manter a hidratação corporal quanto para proteção contra agressões ambientais. De fato, o SC hidrofóbico foi uma importante conquista evolutiva que permitiu a colonização terrestre da terra por intrépidos mamíferos aquáticos1 . É de grande relevância notar que o nosso conhecimento atual da função de barreira da pele e do processo de cornificação é amplamente baseado em estudos em camundongos sem pelos, imunocompetentes (ex: Skh1) e pele humana; no entanto, nossos cães de companhia também podem fornecer insights abundantes.2 Modelos de camundongos projetados (por exemplo, nocautes Pnlp1 e Nipal4) de ictiose congênita autossômica recessiva (ARCI) normalmente são letais no nascimento, enquanto cães com ARCI comparáveis vivem vidas saudáveis apesar da descamação excessiva.3, 4 Já bem estabelecido que algumas doenças espontâneas em cães (por exemplo, dermatite atópica) imitam as condições humanas mais do que modelos de camundongos induzidos quimicamente ou geneticamente.5 Esta revisão enfoca esses distúrbios em cães e, quando apropriado, o condições comparáveis em humanos.
Assuntos
Doenças do Cão , Ictiose , Animais , Diferenciação Celular , Doenças do Cão/genética , Cães , Células Epidérmicas , Epiderme , Ictiose/genética , Ictiose/veterinária , PeleRESUMO
BACKGROUND: It has long been speculated that sterile granulomatous dermatitis and lymphadenitis (SGDL) occurs in adult dogs. However, only three published case reports exist. HYPOTHESIS/OBJECTIVES: To describe clinical presentation, identify breed predispositions, and assess treatment and outcomes of adult dogs with the histopathological diagnosis of SGDL. ANIMALS: Included are 90 dogs with biopsies submitted to a veterinary teaching hospital with a histopathological diagnosis consistent with SGDL, from 2004 to 2018, of which 35 had medical records available for review. METHODS: Data were analysed retrospectively from histopathology submission forms, medical records, surveys and telephone calls. Scoring systems were created to aid statistical analysis of outcomes. RESULTS: Havanese dog (P < 0.0001), Australian shepherd dog (P < 0.0001), Irish setter (P < 0.0001), Dachshund (P = 0.0002), bichon frise (P = 0.0003) and Maltese dog (P = 0.004) were significantly over-represented breeds. The median age at onset was 1,292 days (3.54 years). Dogs up to five years of age were significantly over-represented (P < 0.01). Of 35 dogs with medical records available for review, the median treatment duration was 60 days and the median time to remission 28 days. Remission status was not established for five dogs but the remaining 30 dogs reached remission. Nineteen dogs remained in complete remission. Recrudescence occurred in 11 dogs (median follow-up 60 days). CONCLUSIONS AND CLINICAL IMPORTANCE: This study shows a close parallel in clinical appearance, histopathological results and clinical behaviour, of both adult and juvenile onset SGDL; therefore, SGDL should be considered as a differential diagnosis for dogs of all ages.
Assuntos
Doenças Autoimunes/veterinária , Celulite (Flegmão)/veterinária , Dermatite/veterinária , Doenças do Cão/tratamento farmacológico , Linfadenite/veterinária , Pele/patologia , Fatores Etários , Animais , Doenças Autoimunes/tratamento farmacológico , Biópsia , Cruzamento , Dermatite/tratamento farmacológico , Cães , Feminino , Glucocorticoides/uso terapêutico , Técnicas Histológicas , Linfadenite/tratamento farmacológico , Masculino , Estudos Retrospectivos , Pele/efeitos dos fármacos , Resultado do TratamentoRESUMO
Mutations in several lipid synthetic enzymes that block fatty acid and ceramide production produce autosomal recessive congenital ichthyoses (ARCIs) and associated abnormalities in permeability barrier homeostasis. However, the basis for the phenotype in patients with NIPAL4 (ichthyin) mutations (among the most prevalent ARCIs) remains unknown. Barrier function was abnormal in an index patient and in canines with homozygous NIPAL4 mutations, attributable to extensive membrane stripping, likely from detergent effects of nonesterified free fatty acid. Cytotoxicity compromised not only lamellar body secretion but also formation of the corneocyte lipid envelope (CLE) and attenuation of the cornified envelope (CE), consistent with a previously unrecognized, scaffold function of the CLE. Together, these abnormalities result in failure to form normal lamellar bilayers, accounting for the permeability barrier abnormality and clinical phenotype in NIPA-like domain-containing 4 (NIPAL4) deficiency. Thus, NIPAL4 deficiency represents another lipid synthetic ARCI that converges on the CLE (and CE), compromising their putative scaffold function. However, the clinical phenotype only partially improved after normalization of CLE and CE structure with topical ω-O-acylceramide because of ongoing accumulation of toxic metabolites, further evidence that proximal, cytotoxic metabolites contribute to disease pathogenesis.
Assuntos
Modelos Animais de Doenças , Epiderme/patologia , Ictiose/patologia , Lipídeos/análise , Mutação , Receptores de Superfície Celular/deficiência , Receptores de Superfície Celular/genética , Adulto , Animais , Cães , Epiderme/metabolismo , Feminino , Homozigoto , Humanos , Ictiose/genética , Ictiose/metabolismo , Masculino , Linhagem , FenótipoRESUMO
BACKGROUND: Ischaemic dermatopathy encompasses a poorly understood subset of canine diseases that share similar clinical and histological features. Very little information is currently available regarding population characteristics, progression and outcome. HYPOTHESIS/OBJECTIVES: This study aimed to describe the clinical features and therapeutic outcomes of ischaemia dermatopathy, excluding familial dermatomyositis, using cases diagnosed by histopathological analysis. ANIMALS: One hundred and seventy-seven cases submitted for histopathological analysis between 2005 and 2016 met inclusion criteria, of which 93 had complete medical records available. METHODS AND MATERIALS: Both records and pointed surveys were used to retrieve information. Scoring systems were created to subjectively evaluate clinical outcomes and likelihood of a vaccine association. RESULTS: Of 177 cases, toy and miniature poodles, Chihuahuas, Maltese, Yorkshire terriers and Jack Russell terriers were significantly over-represented (P < 0.001). Of the 93 cases for which historical data were obtained, median age at skin biopsy was five years (0.42-13 years) and median body weight was 7.3 kg (range 1.32-50.3 kg). The condition in 45 dogs (48.3%) was found likely to be associated with vaccination. Younger ages (P = 0.011) and higher body weights (P = 0.003) were positively correlated with greater likelihood of vaccination. Body weight <10 kg (P = 0.0045) and older ages (P = 0.0048) were significantly associated with worse outcomes. CONCLUSIONS AND CLINICAL IMPORTANCE: This study provides support for breed predispositions and identifies potential prognostic factors. Importantly, over half of the cases were considered unlikely to be vaccine-associated, demonstrating the need to investigate other underlying causes of this condition.
Assuntos
Doenças do Cão/patologia , Isquemia/veterinária , Dermatopatias/veterinária , Envelhecimento , Animais , Peso Corporal , Cães , Isquemia/patologia , Dermatopatias/etiologia , Dermatopatias/patologia , Vacinação/efeitos adversosRESUMO
BACKGROUND: Canine acute eosinophilic dermatitis with oedema (CAEDE) and sterile neutrophilic dermatosis have overlapping clinical and histopathological features. HYPOTHESIS/OBJECTIVES: The objective of this study was to identify features that differentiate these entities. ANIMALS: Forty dogs. METHODS AND MATERIALS: Retrospective case series. Forty cases with diagnoses of either CAEDE and/or sterile neutrophilic dermatosis were included based on histopathological review. Medical records (29 of 40 dogs) were reviewed for clinical findings and historical data. Commercially available immunohistochemical stains for granulocytes and a Luna stain were performed (40 of 40 dogs) to assess the granulocytic infiltrate. RESULTS: Nineteen cases had been previously diagnosed as CAEDE, seven cases had been designated as sterile neutrophilic dermatosis and 14 cases had overlapping features. Based on review and receiver operating characteristic (ROC) curve analysis, 30 cases with >12% eosinophils, enumerated by Luna staining, were diagnosed as eosinophilic dermatitis and oedema. Ten cases were diagnosed as sterile neutrophilic dermatosis. Dogs with CAEDE frequently had gastrointestinal signs (24 of 30;80%) and pruritus (11 of 30;33%). In dogs with sterile neutrophilic dermatosis, five of 10 (50%) had diagnoses of or histories compatible with immune-mediated polyarthropathy. CONCLUSIONS AND CLINICAL IMPORTANCE: In this case series, CAEDE was encountered more frequently than neutrophilic dermatosis and could be distinguished by the eosinophilic infiltrate, aided by a Luna stain. Concurrent arthralgia was more frequently identified with neutrophilic dermatosis. It remains unclear whether CAEDE and sterile neutrophilic dermatosis are separate disease entities or varied manifestations of the same disease.
Assuntos
Dermatite/veterinária , Doenças do Cão/diagnóstico , Edema/veterinária , Pele/imunologia , Síndrome de Sweet/veterinária , Animais , Biópsia , Dermatite/diagnóstico , Dermatite/imunologia , Doenças do Cão/imunologia , Cães , Edema/etiologia , Edema/imunologia , Feminino , Masculino , Estudos Retrospectivos , Pele/patologia , Síndrome de Sweet/fisiopatologiaRESUMO
BACKGROUND: The Burkholderia cepacia complex (Bcc) is an emerging cause of opportunistic infections. Deep pyoderma associated with Bcc infection has been reported previously in dogs receiving ciclosporin. OBJECTIVE: To report the clinical and histopathological features of four additional cases of Bcc dermatitis in dogs, one of which progressed to septicaemia. ANIMALS: Four dogs with a skin culture yielding growth of Bcc and skin biopsies for histopathological investigation. METHODS AND MATERIALS: Retrospective review of medical records and skin biopsies and PCR for Burkholderia on DNA extracted from paraffin-embedded skin and liver to confirm Bcc sepsis. RESULTS: Three different breeds and one mixed breed dog were represented. Two dogs were receiving ciclosporin and one was receiving oclacitinib. One dog had no evidence of immunosuppression. One dog was bathed two days prior to onset of skin lesions. Three dogs presented with dorsally orientated ulcers, crusts and draining tracts; one dog had infection localized to a surgical site. The main histological feature from skin biopsies was severe neutrophilic folliculitis and furunculosis with marked neutrophilic to pyogranulomatous dermatitis. Intracellular Gram-negative and Warthin-Starry positive rods were present in three of four cases. Three dogs were successfully treated with systemic fluoroquinolones or trimethoprim sulfamethoxazole. The Bcc isolate in one dog was resistant to all tested systemic antimicrobials. This dog developed septicaemia and was euthanized. CONCLUSIONS AND CLINICAL IMPORTANCE: Bcc skin infections can occur in immunocompetent and immunocompromised dogs. Bcc isolates may be extensively antimicrobial resistant, presenting a challenge for clinical management. Cutaneous infection may progress to life-threatening sepsis.
Assuntos
Infecções por Burkholderia/veterinária , Complexo Burkholderia cepacia , Doenças do Cão/microbiologia , Animais , Anti-Infecciosos/uso terapêutico , Infecções por Burkholderia/microbiologia , Infecções por Burkholderia/patologia , Doenças do Cão/patologia , Cães , Hospedeiro Imunocomprometido , Masculino , Reação em Cadeia da Polimerase/veterinária , Estudos Retrospectivos , Pele/microbiologia , Pele/patologiaRESUMO
Toll-like receptor signaling and subsequent activation of NF-κB- and MAPK-dependent genes during infection play an important role in antimicrobial host defense. The YopJ protein of pathogenic Yersinia species inhibits NF-κB and MAPK signaling, resulting in blockade of NF-κB-dependent cytokine production and target cell death. Nevertheless, Yersinia infection induces inflammatory responses in vivo. Moreover, increasing the extent of YopJ-dependent cytotoxicity induced by Yersinia pestis and Yersinia pseudotuberculosis paradoxically leads to decreased virulence in vivo, suggesting that cell death promotes anti-Yersinia host defense. However, the specific pathways responsible for YopJ-induced cell death and how this cell death mediates immune defense against Yersinia remain poorly defined. YopJ activity induces processing of multiple caspases, including caspase-1, independently of inflammasome components or the adaptor protein ASC. Unexpectedly, caspase-1 activation in response to the activity of YopJ required caspase-8, receptor-interacting serine/threonine kinase 1 (RIPK1), and Fas-associated death domain (FADD), but not RIPK3. Furthermore, whereas RIPK3 deficiency did not affect YopJ-induced cell death or caspase-1 activation, deficiency of both RIPK3 and caspase-8 or FADD completely abrogated Yersinia-induced cell death and caspase-1 activation. Mice lacking RIPK3 and caspase-8 in their hematopoietic compartment showed extreme susceptibility to Yersinia and were deficient in monocyte and neutrophil-derived production of proinflammatory cytokines. Our data demonstrate for the first time to our knowledge that RIPK1, FADD, and caspase-8 are required for YopJ-induced cell death and caspase-1 activation and suggest that caspase-8-mediated cell death overrides blockade of immune signaling by YopJ to promote anti-Yersinia immune defense.
Assuntos
Caspase 1/metabolismo , Caspase 8/metabolismo , Imunidade Inata , Sistema de Sinalização das MAP Quinases , NF-kappa B/metabolismo , Animais , Apoptose , Proteínas de Bactérias/genética , Ativação Enzimática , Proteína de Domínio de Morte Associada a Fas/metabolismo , Regulação Enzimológica da Expressão Gênica , Camundongos , Camundongos Transgênicos , Proteína Serina-Treonina Quinases de Interação com Receptores/metabolismo , Yersiniose/microbiologia , Yersinia pseudotuberculosisRESUMO
BACKGROUND: Plectin, a large linker protein found in many tissues, acts to connect components of the cytoskeleton to each other. In the epidermis, plectin binds keratin intermediate filaments to hemidesmosomes. A deficiency of plectin in the skin leads to blister formation in the basal layer and the disease epidermolysis bullosa simplex (EBS). HYPOTHESIS/OBJECTIVES: To describe a novel blistering disease that arose spontaneously in a litter of puppies. ANIMALS: Two female and one male 20-day-old Eurasier puppies, from a litter of six, were presented for evaluation of failure to thrive and then euthanized due to poor prognosis. The puppies had ulcers on the lips, tongue, nasal planum, paw pads and abdomen. RESULTS: Immunolabelling on frozen skin for basement membrane proteins revealed patchy and weak to absent staining for plectin as compared with strong linear staining in normal dogs. Ultrastructurally, hemidesmosomes were irregularly shaped and had loss of distinction between inner and outer plaques. Pedigree analysis supported an autosomal recessive mode of inheritance. A premature stop codon was discovered in exon 27 of PLEC that resulted in the production of a severely truncated protein. CONCLUSION: The study describes the first documented spontaneous EBS associated with a PLEC variant in domestic animals.
Assuntos
Códon sem Sentido/genética , Doenças do Cão/genética , Epidermólise Bolhosa Simples/veterinária , Plectina/genética , Animais , Códon sem Sentido/fisiologia , Doenças do Cão/patologia , Cães/genética , Epidermólise Bolhosa Simples/genética , Epidermólise Bolhosa Simples/patologia , Feminino , Masculino , Linhagem , Plectina/fisiologia , Irmãos , Pele/patologiaRESUMO
Although keratosis pilaris (KP) is common, its etiopathogenesis remains unknown. KP is associated clinically with ichthyosis vulgaris and atopic dermatitis and molecular genetically with filaggrin-null mutations. In 20 KP patients and 20 matched controls, we assessed the filaggrin and claudin 1 genotypes, the phenotypes by dermatoscopy, and the morphology by light and transmission electron microscopy. Thirty-five percent of KP patients displayed filaggrin mutations, demonstrating that filaggrin mutations only partially account for the KP phenotype. Major histologic and dermatoscopic findings of KP were hyperkeratosis, hypergranulosis, mild T helper cell type 1-dominant lymphocytic inflammation, plugging of follicular orifices, striking absence of sebaceous glands, and hair shaft abnormalities in KP lesions but not in unaffected skin sites. Changes in barrier function and abnormal paracellular permeability were found in both interfollicular and follicular stratum corneum of lesional KP, which correlated ultrastructurally with impaired extracellular lamellar bilayer maturation and organization. All these features were independent of filaggrin genotype. Moreover, ultrastructure of corneodesmosomes and tight junctions appeared normal, immunohistochemistry for claudin 1 showed no reduction in protein amounts, and molecular analysis of claudin 1 was unremarkable. Our findings suggest that absence of sebaceous glands is an early step in KP pathogenesis, resulting in downstream hair shaft and epithelial barrier abnormalities.
Assuntos
Anormalidades Múltiplas/patologia , Doença de Darier/patologia , Epiderme/anormalidades , Sobrancelhas/anormalidades , Cabelo/anormalidades , Proteínas de Filamentos Intermediários/deficiência , Glândulas Sebáceas/anormalidades , Anormalidades Múltiplas/genética , Adulto , Idoso , Claudina-1/metabolismo , Doença de Darier/genética , Dermoscopia , Desmossomos/metabolismo , Epiderme/ultraestrutura , Sobrancelhas/patologia , Feminino , Proteínas Filagrinas , Genótipo , Cabelo/ultraestrutura , Humanos , Proteínas de Filamentos Intermediários/genética , Masculino , Pessoa de Meia-Idade , Mutação/genética , Permeabilidade , Fenótipo , Glândulas Sebáceas/patologia , Glândulas Sebáceas/ultraestrutura , Adulto JovemRESUMO
Breast cancer metastasis is the leading cause of cancer-related deaths in women worldwide. Collagen in the tumor microenvironment plays a crucial role in regulating tumor progression. We have shown that type III collagen (Col3), a component of tumor stroma, regulates myofibroblast differentiation and scar formation after cutaneous injury. During the course of these wound-healing studies, we noted that tumors developed at a higher frequency in Col3(+/-) mice compared to wild-type littermate controls. We, therefore, examined the effect of Col3 deficiency on tumor behavior, using the murine mammary carcinoma cell line 4T1. Notably, tumor volume and pulmonary metastatic burden after orthotopic injection of 4T1 cells were increased in Col3(+/-) mice compared to Col3(+/+) littermates. By using murine (4T1) and human (MDA-MB-231) breast cancer cells grown in Col3-poor and Col3-enriched microenvironments in vitro, we found that several major events of the metastatic process were suppressed by Col3, including adhesion, invasion, and migration. In addition, Col3 deficiency increased proliferation and decreased apoptosis of 4T1 cells both in vitro and in primary tumors in vivo. Mechanistically, Col3 suppresses the procarcinogenic microenvironment by regulating stromal organization, including density and alignment of fibrillar collagen and myofibroblasts. We propose that Col3 plays an important role in the tumor microenvironment by suppressing metastasis-promoting characteristics of the tumor-associated stroma.