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1.
Actas Dermosifiliogr ; 2024 Jul 18.
Article in English, Spanish | MEDLINE | ID: mdl-39032781

ABSTRACT

BACKGROUND AND OBJECTIVE: subcutaneous panniculitis-like T-cell lymphoma (SPTCL) is a rare cytotoxic T-cell lymphoma with indolent behavior, mostly present in women and associated with immunological diseases whose pathogenic background is still poorly understood. SPTCL is associated with lupus erythematosus panniculitis (LEP) and histologically misdiagnosed. OBJECTIVES: the aim of our study was to identify mutations affecting the pathogenesis of both SPTCL and LEP. MATERIALS AND METHODS: we studied a total of 10 SPTCL and 10 LEP patients using targeted Next Generation Sequencing and pyrosequencing. Differences in gene expression between molecular subgroups were investigated using NanoString technology. Clinical data were collected, and correlations sought with the molecular data obtained. RESULTS: the mutational profile of SPTCL and LEP is different. We identified fewer pathogenic mutations than previously reported in SPTCL, noting a single HAVCR2-mutated SPTCL case. Interestingly, 40% of our SPTCL cases showed the pathogenic TP53 (p.Pro72Arg) (P72R) variant. Although cases showing HAVCR2 mutations or the TP53 (P72R) variant had more severe symptomatic disease, none developed hemophagocytic syndrome (HPS). Furthermore, TP53 (P72R)-positive cases were characterized by a lower metabolic signaling pathway and higher levels of CD28 expression and Treg signaling genes. In addition, 30% of our cases featured the same mutation (T735C) of the epigenetic modificatory gene DNMT3A. None of the LEP cases showed mutations in any of the studied genes. CONCLUSIONS: the mutational landscape of SPTCL is broader than previously anticipated. We describe, for the first time, the involvement of the TP53 (P72R) pathogenic variant in this subgroup of tumors, consider the possible role of different genetic backgrounds in the development of SPTCL, and conclude that LEP does not follow the same pathogenic pathway as SPTCL.

5.
Actas Dermosifiliogr ; 113(4): 388-400, 2022 Apr.
Article in English, Spanish | MEDLINE | ID: mdl-35623729

ABSTRACT

The study of subungual melanocytic lesions can present challenges because of the clinical and histologic characteristics of the nail unit and the difficulty of performing nail biopsies and processing specimens. These lesions can be even more challenging in children due to differences in clinical and epidemiological profiles between the adult and pediatric populations. Many of the clinical features of subungual melanocytic lesions that would raise alarm in an adult do not have the same implications in children. Consensus is also lacking on when a nail biopsy is needed to rule out malignancy in the pediatric setting. In view of these considerations and the rarity of subungual melanoma in childhood, the recommended approach in most cases is a watch-and-wait strategy. Subungual melanocytic lesions in children may also show atypical histopathologic features that are not necessarily associated with aggressive behavior. Subungual melanoma is very rare in childhood, with just 21 cases described to date. None of the patients developed visceral metastasis or died as a result and the diagnosis was controversial in many of the cases. Considering the above and the significantly higher frequency and particular characteristics of longitudinal melanonychia with a benign etiology in children, subungual melanocytic lesions should be managed differently in this setting than in adults. In most cases, a watch-and-wait approach is the most appropriate strategy.


Subject(s)
Melanoma , Nail Diseases , Adult , Biopsy , Child , Humans , Melanocytes/pathology , Melanoma/diagnosis , Melanoma/epidemiology , Melanoma/pathology , Nail Diseases/diagnosis , Nail Diseases/epidemiology , Nail Diseases/pathology , Nails
6.
Actas dermo-sifiliogr. (Ed. impr.) ; 113(4): 388-400, Abr. 2022. ilus, tab
Article in Spanish | IBECS | ID: ibc-206453

ABSTRACT

Debido a las particularidades anatómicas clínicas e histológicas del aparato ungueal, y a las dificultades inherentes a la obtención y procesado de las biopsias ungueales, el estudio de las lesiones melanocíticas subungueales no suele ser una tarea sencilla. Además, en el caso de las lesiones melanocíticas subungueales de la edad pediátrica, hay que añadir las peculiaridades de las características clínicas y epidemiológicas propias de esta edad. En la infancia, muchos de los signos clínicos que son considerados de alarma en el adulto no han demostrado tener la misma validez, y no existe un claro consenso respecto a cuándo realizar una biopsia ungueal para descartar patología melanocítica maligna. Esto, unido al carácter excepcional del melanoma subungueal pediátrico, hacen que en la mayoría de los casos se recomiende exclusivamente la observación y el seguimiento. Por otro lado, las lesiones melanocíticas subungueales pediátricas pueden mostrar características histopatológicas atípicas, sin que ello implique un comportamiento clínico agresivo. El melanoma subungueal es una entidad excepcional, con solo 21 casos descritos hasta la fecha. Cabe destacar que ninguno de los casos de melanoma subungueal pediátrico descritos hasta la fecha presentó afectación metastásica visceral, ni tampoco ocasionó la muerte del paciente, y que el diagnóstico es controvertido en muchos de ellos. Por todo ello, y teniendo en cuenta la significativa mayor frecuencia de lesiones melanocíticas benignas subyacentes a melanoniquias longitudinales en la edad pediátrica, así como las peculiaridades clínicas de las mismas, el manejo de estas lesiones debe ser diferente al de las melanoniquias del adulto, siendo la observación la actitud más adecuada en la gran mayoría de los casos (AU)


The study of subungual melanocytic lesions can present challenges because of the clinical and histologic characteristics of the nail unit and the difficulty of performing nail biopsies and processing specimens. These lesions can be even more challenging in children due to differences in clinical and epidemiological profiles between the adult and pediatric populations. Many of the clinical features of subungual melanocytic lesions that would raise alarm in an adult do not have the same implications in children. Consensus is also lacking on when a nail biopsy is needed to rule out malignancy in the pediatric setting. In view of these considerations and the rarity of subungual melanoma in childhood, the recommended approach in most cases is a watch-and-wait strategy. Subungual melanocytic lesions in children may also show atypical histopathologic features that are not necessarily associated with aggressive behavior. Subungual melanoma is very rare in childhood, with just 21 cases described to date. None of the patients developed visceral metastasis or died as a result and the diagnosis was controversial in many of the cases. Considering the above and the significantly higher frequency and particular characteristics of longitudinal melanonychia with a benign etiology in children, subungual melanocytic lesions should be managed differently in this setting than in adults. In most cases, a watch-and-wait approach is the most appropriate strategy (AU)


Subject(s)
Humans , Child , Nail Diseases/pathology , Skin Neoplasms/pathology , Melanoma/pathology , Biopsy
7.
Actas dermo-sifiliogr. (Ed. impr.) ; 113(4): t388-t400, Abr. 2022.
Article in Spanish | IBECS | ID: ibc-206454

ABSTRACT

The study of subungual melanocytic lesions can present challenges because of the clinical and histologic characteristics of the nail unit and the difficulty of performing nail biopsies and processing specimens. These lesions can be even more challenging in children due to differences in clinical and epidemiological profiles between the adult and pediatric populations. Many of the clinical features of subungual melanocytic lesions that would raise alarm in an adult do not have the same implications in children. Consensus is also lacking on when a nail biopsy is needed to rule out malignancy in the pediatric setting. In view of these considerations and the rarity of subungual melanoma in childhood, the recommended approach in most cases is a watch-and-wait strategy. Subungual melanocytic lesions in children may also show atypical histopathologic features that are not necessarily associated with aggressive behavior. Subungual melanoma is very rare in childhood, with just 21 cases described to date. None of the patients developed visceral metastasis or died as a result and the diagnosis was controversial in many of the cases. Considering the above and the significantly higher frequency and particular characteristics of longitudinal melanonychia with a benign etiology in children, subungual melanocytic lesions should be managed differently in this setting than in adults. In most cases, a watch-and-wait approach is the most appropriate strategy (AU)


Debido a las particularidades anatómicas clínicas e histológicas del aparato ungueal, y a las dificultades inherentes a la obtención y procesado de las biopsias ungueales, el estudio de las lesiones melanocíticas subungueales no suele ser una tarea sencilla. Además, en el caso de las lesiones melanocíticas subungueales de la edad pediátrica, hay que añadir las peculiaridades de las características clínicas y epidemiológicas propias de esta edad. En la infancia, muchos de los signos clínicos que son considerados de alarma en el adulto no han demostrado tener la misma validez, y no existe un claro consenso respecto a cuándo realizar una biopsia ungueal para descartar patología melanocítica maligna. Esto, unido al carácter excepcional del melanoma subungueal pediátrico, hacen que en la mayoría de los casos se recomiende exclusivamente la observación y el seguimiento. Por otro lado, las lesiones melanocíticas subungueales pediátricas pueden mostrar características histopatológicas atípicas, sin que ello implique un comportamiento clínico agresivo. El melanoma subungueal es una entidad excepcional, con solo 21 casos descritos hasta la fecha. Cabe destacar que ninguno de los casos de melanoma subungueal pediátrico descritos hasta la fecha presentó afectación metastásica visceral, ni tampoco ocasionó la muerte del paciente, y que el diagnóstico es controvertido en muchos de ellos. Por todo ello, y teniendo en cuenta la significativa mayor frecuencia de lesiones melanocíticas benignas subyacentes a melanoniquias longitudinales en la edad pediátrica, así como las peculiaridades clínicas de las mismas, el manejo de estas lesiones debe ser diferente al de las melanoniquias del adulto, siendo la observación la actitud más adecuada en la gran mayoría de los casos (AU)


Subject(s)
Humans , Child , Nail Diseases/pathology , Skin Neoplasms/pathology , Melanoma/pathology , Biopsy
8.
J Eur Acad Dermatol Venereol ; 36(3): 351-359, 2022 Mar.
Article in English | MEDLINE | ID: mdl-34931722

ABSTRACT

BACKGROUND: Histopathological classification of basal cell carcinoma (BCC) has important prognostic and therapeutic implications, but reproducibility of BCC subtyping among dermatopathologists is poor. OBJECTIVES: To obtain a consensus paper on BCC classification and subtype definitions. METHODS: A panel of 12 recognized dermatopathologists (G12) from nine European countries used a modified Delphi method and evaluated 100 BCC cases uploaded to a website. The strategy involved five steps: (I) agreement on definitions for WHO 2018 BCC subtypes; (II) classification of 100 BCCs using the agreed definitions; (III) discussion on the weak points of the WHO classification and proposal of a new classification with clinical insights; (IV) re-evaluation of the 100 BCCs using the new classification; and (V) external independent evaluation by 10 experienced dermatopathologists (G10). RESULTS: A simplified classification unifying infiltrating, sclerosing, and micronodular BCCs into a single "infiltrative BCC" subtype improved reproducibility and was practical from a clinical standpoint. Fleiss' κ values increased for all subtypes, and the level of agreement improved from fair to moderate for the nodular and the unified infiltrative BCC groups, respectively. The agreement for basosquamous cell carcinoma remained fair, but κ values increased from 0.276 to 0.342. The results were similar for the G10 group. Delphi consensus was not achieved for the concept of trichoblastic carcinoma. In histopathological reports of BCC displaying multiple subtypes, only the most aggressive subtype should be mentioned, except superficial BCC involving margins. CONCLUSIONS: The three BCC subtypes with infiltrative growth pattern, characteristically associated with higher risk of deep involvement (infiltrating, sclerosing, and micronodular), should be unified in a single group. The concise and encompassing term "infiltrative BCCs" can be used for these tumors. A binary classification of BCC into low-risk and high-risk subtypes on histopathological grounds alone is questionable; correlation with clinical factors is necessary to determine BCC risk and therapeutic approach.


Subject(s)
Carcinoma, Basal Cell , Skin Neoplasms , Carcinoma, Basal Cell/pathology , Consensus , Humans , Margins of Excision , Reproducibility of Results , Skin Neoplasms/pathology
9.
Actas dermo-sifiliogr. (Ed. impr.) ; 112(7): 573-585, jul.-ago. 2021. ilus
Article in Spanish | IBECS | ID: ibc-213432

ABSTRACT

El miedo a realizar intervenciones en la uña por el riesgo de distrofia residual, la dificultad de procesado y de interpretación de las biopsias ungueales, así como la falta global de experiencia en este campo han hecho que las melanoniquias ungueales en general (y las lesiones melanocíticas subungueales en particular) sean un tema poco atractivo tanto para dermatólogos como para patólogos. A pesar de la indudable complejidad de este campo, el manejo de las técnicas de biopsia ungueal, el correcto procesado y orientación de las muestras y el conocimiento de las particularidades histológicas del aparato ungueal pueden facilitar mucho esta labor. La biopsia longitudinal escisional ofrece la interpretación histológica más sencilla y tiene bajo riesgo de generar distrofia ungueal, si se realiza correctamente. Los datos clínicos y epidemiológicos son fundamentales: el diagnóstico de melanoma subungueal en la infancia es excepcional, e incluso lesiones con características clínicas y/o histológicas atípicas constituyen, con toda probabilidad, lesiones benignas. La presencia de melanocitos suprabasales y otros hallazgos que serían sospechosos de malignidad en lesiones en otras localizaciones se consideran normales en el aparato ungueal. El melanoma subungueal tiene un patrón lentiginoso en estadios precoces y parece que la presencia de un infiltrado inflamatorio, acompañando a lesiones subungueales lentiginosas atípicas, es uno de los primeros hallazgos diagnósticos de esta lesión (AU)


Both dermatologists and pathologists sometimes find daunting the evaluation of melanonychia (especially subungual melanocytic lesions) because of the fear of performing nail surgery due to the risk of dystrophy, difficulties processing and interpreting nail biopsy specimens, and a general lack of experience in the field. Nevertheless, mastery of nail biopsy techniques, correct processing and orientation of specimens, and familiarity with the histologic particularities of the nail apparatus can attenuate the undoubted complexity and facilitate the tasks involved. Longitudinal excision is the biopsy technique that ensures the simplest histologic interpretation, and it is associated with a low risk of nail dystrophy when performed correctly. Clinical and epidemiological data are crucial. Subungual melanoma in childhood, for instance, is very rare and even lesions with atypical clinical and/or histologic features are probably benign. The presence of suprabasal melanocytes and other findings that would suggest malignancy at other sites are considered normal in the nail apparatus. Subungual melanoma shows a lentiginous pattern in the early stages of disease, and detection of an inflammatory infiltrate accompanying atypical lentiginous subungual lesions would appear to be one of the first diagnostic findings (AU)


Subject(s)
Humans , Biopsy/methods , Nail Diseases/pathology , Melanocytes/pathology , Nevus/pathology , Skin Neoplasms/pathology , Melanoma/pathology
10.
Article in English | MEDLINE | ID: mdl-34053897

ABSTRACT

Both dermatologists and pathologists sometimes find daunting the evaluation of melanonychia (especially subungual melanocytic lesions) because of the fear of performing nail surgery due to the risk of dystrophy, difficulties processing and interpreting nail biopsy specimens, and a general lack of experience in the field. Nevertheless, mastery of nail biopsy techniques, correct processing and orientation of specimens, and familiarity with the histologic particularities of the nail apparatus can attenuate the undoubted complexity and facilitate the tasks involved. Longitudinal excision is the biopsy technique that ensures the simplest histologic interpretation, and it is associated with a low risk of nail dystrophy when performed correctly. Clinical and epidemiological data are crucial. Subungual melanoma in childhood, for instance, is very rare and even lesions with atypical clinical and/or histologic features are probably benign. The presence of suprabasal melanocytes and other findings that would suggest malignancy at other sites are considered normal in the nail apparatus. Subungual melanoma shows a lentiginous pattern in the early stages of disease, and detection of an inflammatory infiltrate accompanying atypical lentiginous subungual lesions would appear to be one of the first diagnostic findings.

11.
Clin Exp Dermatol ; 46(6): 1097-1101, 2021 Aug.
Article in English | MEDLINE | ID: mdl-33713349

ABSTRACT

Azathioprine is an immunosuppressant drug used in many dermatological and nondermatological pathologies. Azathioprine hypersensitivity syndrome (AHS) is a rare idiosyncratic reaction that is not related to dose or thiopurine methyltransferase activity. Up to half of cases of AHS can present with variable cutaneous manifestations besides fever, malaise and other systemic symptoms. It is important to be aware of AHS, as continuance or reintroduction of the drug can led to multiorgan failure and cardiovascular collapse.


Subject(s)
Azathioprine/adverse effects , Drug Hypersensitivity Syndrome/etiology , Drug Hypersensitivity Syndrome/pathology , Immunosuppressive Agents/adverse effects , Skin/pathology , Diagnosis, Differential , Edema/pathology , Humans , Male , Middle Aged , Neutrophils/pathology
12.
Article in English, Spanish | MEDLINE | ID: mdl-33465340

ABSTRACT

Both dermatologists and pathologists sometimes find daunting the evaluation of melanonychia (especially subungual melanocytic lesions) because of the fear of performing nail surgery due to the risk of dystrophy, difficulties processing and interpreting nail biopsy specimens, and a general lack of experience in the field. Nevertheless, mastery of nail biopsy techniques, correct processing and orientation of specimens, and familiarity with the histologic particularities of the nail apparatus can attenuate the undoubted complexity and facilitate the tasks involved. Longitudinal excision is the biopsy technique that ensures the simplest histologic interpretation, and it is associated with a low risk of nail dystrophy when performed correctly. Clinical and epidemiological data are crucial. Subungual melanoma in childhood, for instance, is very rare and even lesions with atypical clinical and/or histologic features are probably benign. The presence of suprabasal melanocytes and other findings that would suggest malignancy at other sites are considered normal in the nail apparatus. Subungual melanoma shows a lentiginous pattern in the early stages of disease, and detection of an inflammatory infiltrate accompanying atypical lentiginous subungual lesions would appear to be one of the first diagnostic findings.

14.
Br J Dermatol ; 2020 Sep 30.
Article in English | MEDLINE | ID: mdl-33000464

ABSTRACT

We fully agree that the interpretation of electron microscopy findings can be challenging, even for experts. Differences between viral pathogens and normal subcellular organelles may be subtle, and some cellular components can masquerade as viruses. The size and shape of the particle shown in our paper fit with other descriptions of SARS-CoV-2, but there may be a bias in interpretation.

17.
Br J Dermatol ; 183(4): 729-737, 2020 10.
Article in English | MEDLINE | ID: mdl-32562567

ABSTRACT

BACKGROUND: Chilblains ('COVID toes') are being seen with increasing frequency in children and young adults during the COVID-19 pandemic. Detailed histopathological descriptions of COVID-19 chilblains have not been reported, and causality of SARS-CoV-2 has not yet been established. OBJECTIVES: To describe the histopathological features of COVID-19 chilblains and to explore the presence of SARS-CoV-2 in the tissue. METHODS: We examined skin biopsies from seven paediatric patients presenting with chilblains during the COVID-19 pandemic. Immunohistochemistry for SARS-CoV-2 was performed in all cases and electron microscopy in one. RESULTS: Histopathology showed variable degrees of lymphocytic vasculitis ranging from endothelial swelling and endotheliitis to fibrinoid necrosis and thrombosis. Purpura, superficial and deep perivascular lymphocytic inflammation with perieccrine accentuation, oedema, and mild vacuolar interface damage were also seen. SARS-CoV-2 immunohistochemistry was positive in endothelial cells and epithelial cells of eccrine glands. Coronavirus particles were found in the cytoplasm of endothelial cells on electron microscopy. CONCLUSIONS: Although the clinical and histopathological features were similar to other forms of chilblains, the presence of viral particles in the endothelium and the histological evidence of vascular damage support a causal relation of the lesions with SARS-CoV-2. Endothelial damage induced by the virus could be the key mechanism in the pathogenesis of COVID-19 chilblains and perhaps also in a group of patients severely affected by COVID-19 presenting with features of microangiopathic damage. What is already known about this topic? Despite the high number of cases of chilblains seen during the COVID-19 pandemic, a definite causative role for SARS-CoV-2 has not yet been proven. Different pathogenetic hypotheses have been proposed, including coagulation anomalies, interferon release and external factors. What does this study add? The demonstration of SARS-CoV-2 in endothelial cells of skin biopsies by immunohistochemistry and electron microscopy confirms that these lesions are part of the spectrum of COVID-19. Virus-induced vascular damage and secondary ischaemia could explain the pathophysiology of COVID-19 chilblains. Our findings support the hypothesis that widespread endothelial infection by SARS-CoV-2 could have a pathogenetic role in the severe forms of COVID-19. Linked Comment: Wetter. Br J Dermatol 2020; 183:611.


Subject(s)
Chilblains/virology , Coronavirus Infections/complications , Endothelium, Vascular/pathology , Pneumonia, Viral/complications , Skin Diseases/virology , Vasculitis/virology , Betacoronavirus/isolation & purification , Betacoronavirus/pathogenicity , Biopsy , COVID-19 , Chilblains/pathology , Child , Coronavirus Infections/pathology , Coronavirus Infections/virology , Endothelial Cells/pathology , Endothelial Cells/ultrastructure , Endothelial Cells/virology , Endothelium, Vascular/virology , Humans , Immunohistochemistry , Microscopy, Electron , Pandemics , Pneumonia, Viral/pathology , Pneumonia, Viral/virology , SARS-CoV-2 , Skin/blood supply , Skin/pathology , Skin/virology , Skin Diseases/pathology , Vasculitis/pathology
18.
Clin Exp Dermatol ; 44(1): 96-98, 2019 Jan.
Article in English | MEDLINE | ID: mdl-29851125

ABSTRACT

A young woman presented with a perianal nodular lesion, which was found to have histopathological findings of hidradenoma papilliferum. The anal skin is an uncommon location for this neoplasm.


Subject(s)
Sweat Gland Neoplasms/pathology , Tubular Sweat Gland Adenomas/pathology , Adult , Female , Humans , Perineum/pathology
20.
J Eur Acad Dermatol Venereol ; 32(8): 1352-1359, 2018 Aug.
Article in English | MEDLINE | ID: mdl-29524269

ABSTRACT

BACKGROUND: Panniculitis occurring in dermatomyositis is uncommon, with only a few cases described in the literature, most of them as case reports. OBJECTIVE: This report describes the clinicopathological and immunohistochemical findings in a series of 18 patients with panniculitis associated with dermatomyositis. METHODS: In each patient, we collected the clinical data of the cutaneous lesions as well as the characteristic clinical and laboratory findings. A series of histopathologic findings was recorded in the biopsy of each patient. A panel of antibodies was used in some cases to investigate the immunophenotype of the infiltrate. Data of treatment and follow-up were also collected. RESULTS: Of the 18 patients, 13 were female and 5 were male, ranging in age from 13 to 74 years (median, 46.4 years). In addition to panniculitis, all patients presented pathognomonic cutaneous findings of DM and reported proximal muscle weakness prior to the diagnosis of panniculitis. Muscle biopsy was performed in 17 patients and MRI in one, all with the diagnosis of inflammatory myopathy. None of the patients presented any associated neoplasia. Panniculitis lesions were located in the upper or lower limbs. Histopathology showed a mostly lobular panniculitis with lymphocytes as the main component of the infiltrate. Most cases showed also numerous plasma cells and lymphocytes surrounding necrotic adipocytes (rimming) were frequently seen. Lymphocytic vasculitis and abundant mucin interstitially deposited between collagen bundles of the dermis were also frequent findings. Late-stage lesions showed hyaline necrosis of the fat lobule and calcification. Immunohistochemistry demonstrated that most lymphocytes of the infiltrate were T-helper lymphocytes, with some B lymphocytes in the lymphoid aggregates and small clusters of CD-123-positive plasmacytoid dendritic cells in the involved fat lobule. CONCLUSION: Panniculitis in dermatomyositis is rare. Histopathologic findings of panniculitis dermatomyositis are identical to those of lupus panniculitis. Therefore, the final diagnosis requires clinic-pathologic correlation.


Subject(s)
Dermatomyositis/metabolism , Dermatomyositis/pathology , Panniculitis/metabolism , Panniculitis/pathology , Adolescent , Adult , Aged , B-Lymphocytes/pathology , Biopsy , Dendritic Cells/metabolism , Dendritic Cells/pathology , Dermatomyositis/complications , Female , Humans , Interleukin-3 Receptor alpha Subunit/metabolism , Male , Middle Aged , Muscle, Skeletal/pathology , Panniculitis/complications , T-Lymphocytes, Helper-Inducer/pathology , Young Adult
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