RESUMO
BACKGROUND: Sarcoidosis is a multisystemic disease characterized by granulomatous inflammation. Sarcoidosis often poses a diagnostic challenge owing to its nonspecific or mild clinical features. In 20-35% of cases, sarcoidosis initially presents on skin. However, skin lesions commonly mimic dermatological conditions. Therefore, it is important to not underestimate the skin manifestations and perform histopathological examinations to make a timely diagnosis. CASE PRESENTATION: We present two cases of 33-year-old Caucasian female patients with orange-red macules and plaques that developed in the eyebrow area 1 and 6 years after microblading, respectively. Histopathological examination confirmed a diagnosis of sarcoidosis. The lymph nodes and lungs were also affected in both patients. CONCLUSION: Our two reports suggest that an esthetic procedure involving dermal or subcutaneous injection of foreign materials can trigger the development of cutaneous and systemic sarcoidosis. However, this relationship has not been described yet. Physicians should, therefore, be aware of this complication to properly evaluate and treat such patients in a timely manner.
Assuntos
Sarcoidose , Humanos , Feminino , Adulto , Sarcoidose/diagnóstico , Sarcoidose/patologia , Dermatopatias/patologia , Dermatopatias/etiologiaRESUMO
Lichen planus (LP) is a chronic inflammatory disease of the skin and mucous membranes. The disease usually affects adults and is only rarely encountered in children. Typically, skin lesions include violaceous, polygonal, flat papules and plaques, affecting predilection sites such as the wrists, ankles, and lower back. However, clinical presentation can be heterogeneous and is often atypical in children. Various precipitating factors are known to play an important role in the pathogenesis of lichen planus, some of which may also be coincidental. LP occurring after an infection with Mycoplasma pneumoniae is a rare occurrence. We present the case of a 13-year-old boy with pruritic papular skin lesions on the extremities and trunk. In view of the clinical and histopathological findings, LP exanthematicus was diagnosed. To the best of our knowledge, our case is the first of pediatric exanthematous LP after M. pneumoniae infection that has been reported so far.
Assuntos
Líquen Plano , Mycoplasma pneumoniae , Masculino , Adulto , Humanos , Criança , Adolescente , Líquen Plano/complicações , Líquen Plano/diagnóstico , Pele/patologiaRESUMO
Q fever is a rare worldwide zoonosis, caused by the rickettsial bacteria Coxiella burnetii. There are many clinical manifestations of infection, but the most common ones are fever, atypical pneumonia, and/or liver disease. Cutaneous involvement, however, is not a typical feature of Q fever, but it is nevertheless present in up to 20% of cases. We present a 42-year-old male patient with Q fever and erythema exudativum multiforme (EEM)-like parainfectious exanthema, which to the best of our knowledge has not been described before. We recommend considering Coxiella burnetii infection in the differential diagnosis of an EEM-like rash in a patient with an unexplained or "query" fever.
Assuntos
Coxiella burnetii , Exantema , Febre Q , Masculino , Humanos , Adulto , Febre Q/complicações , Febre Q/diagnóstico , Febre Q/microbiologia , Exantema/diagnóstico , Exantema/etiologia , Diagnóstico Diferencial , Eritema/diagnósticoRESUMO
Mycobacterium chelonae is a rapidly growing nontuberculous mycobacteria that is a rare cause of cutaneous infections in both immunocompromised and immunocompetent patients. The clinical presentation is heterogeneous and non-specific, and therefore, despite an increasing incidence of these infections, patients are often misdiagnosed. Here we present the case of an immunocompromised 73-year-old female patient that developed tender, erythematous, violaceous to brownish papules and nodules on both the anterior and posterior aspects of her left lower leg. A histopathological examination revealed acid-fast bacilli, and a tissue culture identified M. chelonae. Disease resolution was achieved with long-term targeted antibiotic therapy based on susceptibility testing.
Assuntos
Infecções por Mycobacterium não Tuberculosas , Mycobacterium chelonae , Dermatopatias Bacterianas , Idoso , Feminino , Humanos , Hospedeiro Imunocomprometido , Perna (Membro) , Infecções por Mycobacterium não Tuberculosas/diagnóstico , Infecções por Mycobacterium não Tuberculosas/tratamento farmacológico , Dermatopatias Bacterianas/diagnóstico , Dermatopatias Bacterianas/microbiologiaRESUMO
Pretibial pruritic papular dermatitis (PPPD) is a clinical entity first described in 2006. The etiology is uncertain; however, gentle chronic rubbing is likely to be the reason for the skin reaction. Pretibial pruritic lesions may reflect many different systemic diseases and dermatoses. We present a 61-year-old patient with a 2-year history of pruritic pretibial xerosis, keratotic erythematous to brownish papules, and excoriations. Differential diagnosis excluded papular mucinosis, myxoedema, stasis dermatitis, lichen simplex chronicus, prurigo nodularis, lichen amyloidosis, and lichen planus. Regarding clinical-histological correlation, we confirmed a diagnosis of PPPD.
Assuntos
Dermatoses da Perna/diagnóstico , Dermatoses da Perna/etiologia , Prurido/diagnóstico , Prurido/etiologia , Diagnóstico Diferencial , Feminino , Humanos , Dermatoses da Perna/terapia , Pessoa de Meia-Idade , Prurido/terapiaRESUMO
Tinea incognita is an atypical presentation of fungal infection of the skin, the clinical presentation of which has been modified by misuse of topical corticosteroids or calcineurin inhibitors. Such dermatophyte infections often have an atypical clinical presentation and are difficult to diagnose, but with the rise of immunosuppressive drugs and self-prescribed topical therapies, they are becoming increasingly prevalent. Here we report the case of a 68-year-old male patient with a history of psoriasis, presenting with erythematous scaly lesions, that did not respond to conventional treatment for psoriasis, as would be expected. A diagnosis of tinea incognita was made with histopathological examination with periodic acid-Schiff stain of a skin biopsy sample. This case highlights the fact that dermatophyte infections are widespread but sometimes neglected and can occur concomitantly with other dermatoses.
Assuntos
Tinha , Idoso , Humanos , Masculino , Psoríase/complicações , Tinha/complicações , Tinha/patologiaRESUMO
Hand, foot, and mouth disease is a highly contagious disease that predominantly affects children under the age of five. The illness is much less common in adults and often presents with atypical skin lesions. Here we describe the case of a 19-year-old healthy, immunocompetent male patient with atypical clinical presentation, with a macular rash on the scalp, palms, soles, and shins, and with minimal lesions in the oral cavity. The diagnosis of hand, foot, and mouth disease was confirmed by isolation of coxsackievirus A6 from a vesicle smearobtained on the right sole. The skin lesions resolved spontaneously in 1 week. This case emphasizes the underestimated fact that hand, foot, and mouth disease can also occur in adults, in either typical or frequently atypical form, and it highlights the role of coxsackievirus A6. Together with the case presentation, a review of the literature describing the disease in adults is presented.
Assuntos
Infecções por Coxsackievirus/virologia , Enterovirus Humano A/isolamento & purificação , Doença de Mão, Pé e Boca/virologia , Doença de Mão, Pé e Boca/terapia , Humanos , Imunocompetência , Masculino , Adulto JovemRESUMO
We investigated the feasibility and diagnostic agreement of a virtual slide system (VSS) in teledermatopathology. Forty-six biopsy specimens from inflammatory skin diseases were selected and scanned with a VSS at the Research Unit of Teledermatology, Medical University of Graz, Graz, Austria. Images were stored on a virtual slide server on which a specific Web application suited for telepathology (http://telederm.org/research/dermatopath/) runs. Twelve teleconsultants from 6 different countries reviewed the 46 cases, working directly on the Web application. Telediagnoses agreed with gold standard and conventional diagnosis with an average of 73% and 74%, respectively. Complete concordance among all teleconsultants with gold standard and conventional diagnosis was found in 20% of the cases. In 10 cases in which complete clinical data were missing, the average agreement of telediagnosis with gold standard diagnosis and conventional diagnosis decreased to 65% and 66%, respectively. Only 3 of 4 cases of inflammatory skin diseases were correctly diagnosed remotely with VSS. The system that we have used, despite its usability, is not completely feasible for teledermatopathology of inflammatory skin disease. Moreover, the performance seems to have been influenced by the availability of complete clinical data and by the intrinsic difficulty of the pathology of inflammatory skin diseases.
Assuntos
Dermatopatias/patologia , Telepatologia/métodos , Telepatologia/normas , Interface Usuário-Computador , Adolescente , Adulto , Idoso , Idoso de 80 Anos ou mais , Biópsia/métodos , Criança , Dermatologia/métodos , Estudos de Viabilidade , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Variações Dependentes do Observador , Dermatopatias/diagnósticoRESUMO
Lichen striatus is a self-limited, lichenoid eruption particularly common in children. The lesions are located on extremities and less commonly on the trunk, and they follow the developmental lines of Blaschko. The etiology of lichen striatus is as yet unknown. It has been observed after infection or immunization in atopic patients and in siblings. The authors report on a 15-month-old girl that developed lichen striatus along the Blaschko lines on the trunk and one extremity after receiving the combined vaccine against measles, mumps, and rubella. Six months later, complete resolution of the skin lesions occurred without any treatment, leaving only slightly hypopigmented macules on the extremity.
Assuntos
Erupções Liquenoides/induzido quimicamente , Vacina contra Sarampo-Caxumba-Rubéola/efeitos adversos , Feminino , Humanos , Lactente , Erupções Liquenoides/patologia , Pele/patologiaRESUMO
Follicular mucinosis is characterized by mucin deposits within the hair follicles and sebaceous glands. It can occur as a primary idiopathic benign disorder; it can be found as an incidental phenomenom in rare cases of different dermatoses; or it can arise as a secondary symptom of a malignant disorder, most commonly mycosis fungoides. Youth and localization in a single area used to be regarded as indicative of the benign nature of follicular mucinosis. However, recent reports demonstrate that no clear-cut criteria allow for the differentiation of idiopathic from lymphoma-associated follicular mucinosis. We report the case of a 16-year old girl who presented with a 2-year history of a single, slightly pruritic, erythematous patch on the left side of the neck. Different local treatments (local corticosteroids, antibiotics, antifungal ointments and moisturizers) were ineffective. Overall, she was healthy. Histopathological examination of the lesion showed the typical histological picture of follicular mucinosis.
Assuntos
Mucinose Folicular/patologia , Adolescente , Epiderme/patologia , Feminino , Humanos , Hiperplasia , Pescoço/patologiaRESUMO
We performed a multicentre study to test the validity of teledermoscopy for diagnosing acral melanoma and to evaluate inter-observer agreement on the classification of acral melanocytic lesions. Dermoscopic images of 77 acral melanocytic lesions (71 common melanocytic naevi and 6 melanomas) were sent by email to 11 dermatologists with different degrees of experience in dermoscopy. The observers analysed the images on a computer monitor to diagnose acral melanoma or atypical lesions and to categorize all lesions. All 11 observers, regardless of their degree of experience, obtained high values for sensitivity (mean 0.91, SD 0.09) and specificity (mean 0.95, SD 0.04) with regard to the diagnosis of melanoma. The inter-observer agreement was good to excellent (kappa 0.49-0.88) for the categorization of acral melanocytic lesions. All six melanomas were correctly classified as 'atypical pattern' and all observers recommended surgical excision. Teledermoscopy represents a useful tool for the diagnosis of acral melanoma and for the categorization of patterns that suggest benign or potentially malignant acral melanocytic lesions.
Assuntos
Nevo Pigmentado/diagnóstico , Neoplasias Cutâneas/diagnóstico , Telepatologia/métodos , Adolescente , Adulto , Idoso , Criança , Pré-Escolar , Dermoscopia/métodos , Feminino , Humanos , Masculino , Melanoma/diagnóstico , Pessoa de Meia-Idade , Fotografação , Valor Preditivo dos Testes , Sensibilidade e EspecificidadeRESUMO
Figurate erythema can appear in a wide spectrum of dermatological diseases. Rarely, it can present as an atypical manifestation of bullous pemphigoid. Among eosinophilic dermatoses, figurate erythema may appear in Wells syndrome, which has been occasionally reported in association with Toxocara infection. We present the case of an older female patient diagnosed with bullous pemphigoid, who presented with an unusual combination of blisters and figurate erythema outside the area of blister formation. In addition, high blood eosinophilia associated with lymph node and bone marrow eosinophilia was diagnosed and was causally related to Toxocara canis infection. The patient was treated with dapsone for bullous pemphigoid and with albendazole for toxocariosis, with complete regression of all skin lesions and blood eosinophilia. This paper discusses the possible etiopathogenesis of figurate erythema in our patient and summarizes previous clinical and histological findings in bullous pemphigoid and eosinophilic dermatoses presenting with figurate erythema lesions.
Assuntos
Eritema/complicações , Penfigoide Bolhoso/complicações , Toxocara/isolamento & purificação , Toxocaríase/complicações , Idoso , Animais , Antibacterianos/uso terapêutico , Biópsia por Agulha , Dapsona/uso terapêutico , Eritema/diagnóstico , Eritema/tratamento farmacológico , Feminino , Imunofluorescência/métodos , Humanos , Imuno-Histoquímica , Penfigoide Bolhoso/diagnóstico , Penfigoide Bolhoso/tratamento farmacológico , Prognóstico , Toxocaríase/diagnóstico , Toxocaríase/tratamento farmacológico , Resultado do TratamentoRESUMO
We report on a 30-year-old man that was seen by dermatologist for a routine check of melanocytic nevi. During the examination he pointed out a lesion on his upper back, stating that he did not know how long it had been there. Excision was performed and the histopathologic examination showed a dense granulomatous infiltrate in the dermis without ulceration. It turned out to be cutaneous leishmaniasis, the incidence of which is increasing in our immediate vicinity, and therefore it is important to constantly keep it in mind during everyday work at the clinic.
Assuntos
Leishmaniose Cutânea/patologia , Doenças Negligenciadas/patologia , Nevo Pigmentado/patologia , Neoplasias Cutâneas/patologia , Adulto , Biópsia por Agulha , Dermoscopia/métodos , Diagnóstico Diferencial , Humanos , Imuno-Histoquímica , Leishmaniose Cutânea/diagnóstico , Leishmaniose Cutânea/cirurgia , Masculino , Doenças Negligenciadas/diagnóstico , Doenças Negligenciadas/cirurgia , Nevo Pigmentado/diagnóstico , Nevo Pigmentado/cirurgia , Medição de Risco , Neoplasias Cutâneas/diagnóstico , Neoplasias Cutâneas/cirurgiaRESUMO
The authors report 2 cases of cutaneous pseudolymphoma that occurred in 2 young adult patients who referred for relentlessly growing nodules that appeared within 4 to 5 months after the application of a mercury-based tattoo. Systemic symptoms were not present and there was no evidence of lymph node enlargement. Clinically, both lesions were limited to the red, mercury-based areas of the tattoo. Microscopic examination featured a dense cellular infiltrate composed of polytypic T cells in the upper to mid-dermis, coupled with focal interface tissue reaction. Scattered macrophages contained finely granular particles in their cytoplasm. In addition, extracellular pigment particles were also recognized. Collections of epithelioid macrophages were present in both cases and were reminiscent of epithelioid granulomas. This study confirms evidence that, among skin diseases featuring a dense lymphoid infiltrate, cutaneous pseudolymphoma secondary to tattooing is a rare but not exceptional source of diagnostic challenges.
Assuntos
Pseudolinfoma/etiologia , Pseudolinfoma/patologia , Dermatopatias/etiologia , Dermatopatias/patologia , Tatuagem/efeitos adversos , Adulto , Diagnóstico Diferencial , Feminino , Humanos , Tinta , Linfoma/patologia , Masculino , Compostos de Mercúrio/efeitos adversos , Pessoa de Meia-IdadeRESUMO
We describe 5 cases of "compound blue nevus" (CBN) ("superficial blue nevus with prominent intraepidermal dendritic melanocytes," "Kamino nevus"). Dermoscopically in 2 of 4 cases the bluish pigmentation characteristic of blue nevi was centrally replaced by a black lamella, with black dots and brown globules also observed in one case, thus revealing a structural asymmetry suggestive of melanoma. Histopathologically, pigmented parakeratosis was the underlying histopathologic finding of black lamella and dots/globules. Immunohistochemistry highlighted the unique histopathologic feature of CBN, namely, single dendritic melanocytes at the dermoepidermal junction with striking intraepidermal prolongations. Our findings confirm that CBN is a distinctive variant of blue nevus that may mimic cutaneous melanoma both clinically and dermoscopically.