Abstract: Erythroderma consists of erythema and scaling involving most or all of the body surface. This generalized eruption may be idiopathic, drug-induced or secondary to cutaneous or systemic disease. A 71-year-old man is reported presenting generalized erythema and desquamation with deck-chair sign, nail dystrophy, and plantar ulcers associated with loss of local tactile sensitivity. Biopsies from three different sites demonstrated diffuse lymphocytic infiltrate with incipient granulomas. Fite-Faraco staining showed numerous isolated bacilli and globi. The skin smear was positive. Clinical and pathological diagnosis of borderline lepromatous leprosy was confirmed. This report demonstrates that chronic multibacillary leprosy can manifest as erythroderma and thus should be included in the differential diagnosis.

Abstract: Background: Histological and mycological changes during itraconazole use have not been totally established in chromoblastomycosis. Objectives: To evaluate tissue modifications in chromoblastomycosis carriers under itraconazole treatment. Methods: A histological retrospective study of 20 cases of chromoblastomycosis seen at the university hospital at the south of Brazil, during itraconazole 400 mg daily treatment. Patients were classified into two groups: plaque or tumor lesions, and underwent periodic evaluations every four months during three years. Hematoxylin-eosin stain was used to analyze epidermal modifications, inflammatory infiltrate and fibrosis, and Fontana-Masson stain for parasite evaluation. Results: Fontana-Masson stain was superior to hematoxylin-eosin stain in fungal count in the epidermis (mean difference=0.14; p<0.05). The most distinct mycosis tissue responses were registered in the dermis. Epidermal thinning, granulomatous infiltrate decrease or disappearance, fibrosis increase and quantitative/morphological changes occurred during treatment. Study limitations: Patients could not be located to have their current skin condition examined. Conclusion: Parasitic and tissue changes verified in this study can reflect the parasite-host dynamics under itraconazole action.

The authors report a case of cutaneous tuberculosis in a 63-year-old female patient, who had an infiltrated, erythematous-ferruginous plaque of indurated aspect on her right leg and a nonreactive PPD skin test. Diagnosis was made by tissue culture and PCR of skin biopsy material. The treatment was performed with pyrazinamide, rifampicin, isoniazid and ethambutol, with good response.

Intravascular papillary endothelial hyperplasia is a benign vascular lesion caused by proliferation of endothelium. It is reactive to thrombotic or inflammatory stimuli in the vessel wall.We report the case of a 14-yearold male patient with a violet-colored erythematous tumoral lesion of progressive growth in the occipital region. The diagnosis of intravascular papillary endothelial hyperplasia (IPEH) was confirmed by clinical and histopathological findings. Total lesion exeresis was performed with no recurrence up to date. IPEH presents clinical importance due to its clinical and histological resemblance to angiosarcoma. In order to differentiate it from angiosarcoma, distinguishing features of the benign disease should be considered, such as lack of cellular atypia and rare mitotic activity.Prognosis is good.

A esclerodermia localizada (EL) ou morfeia é uma doença crônica do tecido conjuntivo, de provável etiologia autoimune, que tem como base alterações na síntese e deposição do colágeno, representadas clinicamente por lesões cutâneas escleróticas. Algumas placas podem apresentar coloração amarelada ou xantocrômica, causando confusão diagnóstica. Este artigo relata o caso de uma adolescente, com concomitância de lesões eritematosas e xantocrômicas, ambas manifestações clínicas da doença.

Localized scleroderma or morphea is a chronic disease of the connective tissue. Its etiology may be autoimmune and the condition results from a disturbance in collagen synthesis and deposition, clinically represented by sclerotic skin lesions. Some plaques may be yellowish, which can be misleading at diagnosis. This article reports the case of an adolescent girl who concomitantly presented erythematous lesions and yellowish lesions, both of which constitute clinical manifestations of the disease.

Sarcoma de Kaposi é um tumor vascular que afeta a parede dos vasos linfáticos. Possui quatro formas: clássica, endêmica, iatrogênica e associada ao HIV. É uma doença sistêmica, maligna, multifatorial e de curso variável. A apresentação inicial no pênis é rara, e mais observada em pacientes HIV positivos. Em pacientes HIV negativos, os casos que ocorrem nesta região, apresentam-se com pápulas, nódulos, placas e lesões verruciformes, assintomáticas. Para o tratamento da forma clássica, dispõem-se de excisão cirúrgica, crioterapia, eletrocirurgia, laser e radioterapia. Neste trabalho, é relatado um caso raro de um paciente com a forma clássica, em região peniana tratado com sucesso com radioterapia.

Kaposi's sarcoma is a vascular tumor involving the wall of lymphatic vessels. There are four types: classic, endemic, iatrogenic and HIV-associated. It is a systemic, malignant and multifactorial disease and has a variable course. The primary presentation on the penis is uncommon and is mainly observed in HIV-positive patients. In HIV-negative individuals, asymptomatic papules, nodules, plaques and verrucous lesions are found. The treatment for the classic form involves surgery, cryotherapy, electrosurgery, laser and radiation therapy. The authors present a rare case of a patient with the classic form on the penis, who was successfully treated by radiation therapy.

Porocarcinoma écrino é um tumor de pele raro derivado do acrossiríngeo. Quatro casos de porocarcinoma écrino são estudados. Os pacientes tinham idade entre 49 e 64 anos, sendo dois homens e duas mulheres. O tempo de crescimento dos tumores variou de um a 20 anos. As lesões mediam de 1,2 x 2 a 4 x 5 cm e se localizavam nas extremidades ou na face. Dois pacientes apresentavam carcinoma basocelular em sítios diferentes do porocarcinoma écrino. Duas das biópsias foram previamente descritas como poroma écrino; entretanto, malignidade foi observada em todos os casos após excisão ampla. Portanto, em toda biópsia de pele compatível com poroma écrino, deve-se considerar a possibilidade de malignidade.

Eccrine porocarcinoma is an extremely rare skin tumor derived from the acrosyringium. Four cases of eccrine porocarcinoma are described, two males and two females, aged from 49 to 64 years. Tumors grew in an interval of one to 20 years. Lesions ranged from 1.2 x 2 cm to 4 x 5 cm and were on limbs or face. Two patients had basal cell carcinoma in a site different from the eccrine porocarcinoma. Two biopsies were described as eccrine poroma. Malignancy was observed in all cases after wide excision. Therefore, eccrine porocarcinoma should always be considered after a biopsy compatible with eccrine poroma.

Alterações ungueais são queixas muito frequentes nos consultórios dermatológicos. Onicomicoses representam cerca de 50% das onicopatias, daí a importância de se estabelecer o diagnóstico correto antes de se iniciar o tratamento. Neste artigo, relataremos a utilidade de um exame que é de fácil execução pelo clínico, de baixo custo e sensível: esse exame consiste na análise histopatológica da queratina ungueal distal, atualmente já consagrado com o termo clipping.

Onycodystrophies are common problems in dermatologic practice. About 50% of dystrophic nails have a fungal cause, so it is very important to establish a correct diagnosis before treatment. In this article we relate the usefulness of an easydoing exam, free from pain, cheap and sensible. This exam is the histopathology of the nail keratin or nail clipping.

A sarcoidose é doença granulomatosa multissistêmica que geralmente compromete o trato respiratório e os linfonodos hilares. A pele é comumente afetada, mas raramente o couro cabeludo. Dois casos de sarcoidose com lesões no couro cabeludo são relatados: o primeiro, em paciente negra apresentando áreas de alopecia no couro cabeludo associada a outras lesões cutâneas; e o segundo, em paciente branca, portadora de sarcoidose pulmonar, com alopecia como manifestação cutânea isolada. A sarcoidose de couro cabeludo merece especial atenção, pois nos pacientes com essa forma de lesão cutânea existe alta incidência de acometimento sistêmico.

Sarcoidosis is a multi-system granulomatous disease that generally affects the respiratory tract and hilar lymph nodes. The skin is also commonly involved, although cutaneous sarcoidosis on the scalp is rare. Two cases of scalp sarcoidosis are reported: the first presented with patchy alopecia, cutaneous sarcoidosis and also systemic disease in a black patient; the second case is related to an uncommon presentation with alopecia as the single cutaneous manifestation in a Caucasian patient with pulmonary sarcoidosis. Scalp sarcoidosis deserves special attention because there is a high incidence of other systemic lesions with this cutaneous manifestation, thus a careful investigation should be performed in these patients.

FUNDAMENTOS: A biópsia por punch é de grande auxílio no diagnóstico das doenças do couro cabeludo quando avaliada por patologista experiente. O conhecimento das estruturas encontradas no couro cabeludo normal facilita o diagnóstico histopatológico nessa área tão complexa da dermatopatologia. OBJETIVO: Determinar dados quantitativos normais do couro cabeludo de adultos brancos. MÉTODOS: Em 20 necrópsias, 80 fragmentos de couro cabeludo clinicamente normal foram obtidos por punch 4mm. As amostras foram avaliadas em cortes transversais. RESULTADOS: Em fragmentos obtidos de adultos brancos, com idade variando entre 21 e 78 anos, foi possível observar (medianas): 16,5 (12-23) folículos totais; oito (6-9) unidades foliculares; 15 (10-20) folículos terminais; um (0-2) folículo velo; um (0-2,5) trato fibroso; 92,2% de folículos anágenos; 1,6% de catágenos e 6,2% de telógenos. CONCLUSÃO: Além dos resultados apresentados, observaram-se ainda nos indivíduos do sexo masculino: menor número de unidades foliculares, folículos totais e folículos telógenos; e ainda, nas regiões frontal e vértex, maior número de folículos e tratos fibrosos.

BACKGROUND - Punch-biopsy is a great tool for the diagnosis of scalp disorders, however experience is required for the dermatopathologist. Recognizing the standard structures found in normal scalp is very helpful in this aspect. OBJECTIVE - The goal of this study was to determine quantitative data considering normal structures on the scalp of white adults. METHODS - Twenty necropsies were followed by eighty 4mm-punch biopsies of clinically normal scalp. Samples were evaluated by transverse sections. RESULTS - Scalp fragments from white adults, age 21 to 78, demonstrated (medians): 16.5 (12.0-23.0) total follicles; 8.0 (6.0-9.0) follicular units; 15.0 (10.0-20.0) terminal follicles; 1.0 (0.0-2.0) vellus follicle; and 1.0 (0.0-2.5) fibrous tract. Considering the hair cycle phase: 92.2% were in anagen; 1.6% in catagen and 6.2% in telogen. CONCLUSION - Comparing the results, male samples demonstrated fewer follicular units, total and telogen follicles, and higher number of total follicles and fibrous tracts on frontal and vertex area.

A paraqueratose granular é alteração da queratinização, primeiramente descrita em adultos, caracterizada por pápulas e placas hiperqueratósicas nas áreas intertriginosas. Os autores descrevem seis casos de paraqueratose granular em crianças. Um paciente apresentava lesões nas regiões glúteas, dois em ambas as axilas e região cervical (apresentações inéditas na literatura). Três pacientes apresentavam lesões em pregas inguinais. Realizam também revisão da literatura e discutem a possível etiologia dessa rara dermatose.

Granular parakeratosis is an alteration of keratinization that was first described in adults. It is characterized by hiperkeratotic plaques and papules in intertriginous areas. The authors describe six cases of granular parakeratosis in children. One patient had lesions on the buttocks; two children presented papules in both axillae and cervical region (presentations never described before in the literature). The remaining three patients presented with lesions in the inguinal folds. Review of the literature and discussion on the pathogenesis of this rare dermatosis are presented.

FUNDAMENTOS: A caracterização histológica do folículo piloso normal em humanos é escassa na literatura, considerando que o reconhecimento da arquitetura folicular normal e suas variações nas diversas áreas do couro cabeludo é fundamental para o estudo das doenças do couro cabeludo. OBJETIVOS: Analisar fragmentos do couro cabeludo normal em indivíduos de raça branca quanto à área, os diâmetros máximo e mínimo dos folículos anágenos terminais. MÉTODOS: Vinte necrópsias de indivíduos de raça branca, com idade variando de 20 a 78 anos, foram acompanhadas da coleta de biópsias por punch de 4mm de diâmetro em quatro áreas do couro cabeludo. Os casos foram divididos conforme o sexo em dois grupos, com 10 casos cada. A área e os diâmetros máximo e mínimo dos folículos anágenos terminais foram determinados por análise computadorizada das imagens de cortes transversais da microscopia óptica. Os resultados obtidos foram comparados entre os sexos e os locais de coleta. RESULTADOS: Os resultados numéricos das áreas e diâmetro máximo e mínimo são expostos e comparados. CONCLUSÃO: Não houve diferença estatisticamente significativa entre o diâmetro máximo e a área folicular nas diversas regiões do couro cabeludo; entretanto, foram evidenciadas dimensões de folículos anágenos terminais maiores no sexo masculino do que no feminino.

BACKGROUND: Histological description of normal human hair follicle has scarce literature. Recognizing normal scalp follicle and its variability throughout the scalp is fundamental to study scalp disorders. OBJECTIVES: To evaluate normal scalp samples in Caucasians considering cross-section area, maximum and minimum diameters of terminal anagen follicles. METHODS: Twenty necropsies of Caucasian individuals (10M, 10F) were followed by a 4mm punch biopsy of 4 scalp areas. Transverse sections were evaluated by light microscopy. Terminal anagen follicle cross-section area, maximum and minimum diameters were determined by computer image analysis. Results were compared between sexes and scalp areas. RESULTS: Follicular area and maximum and minimum diameters are presented. CONCLUSION: No statistically significant differences were observed in follicular maximum diameter and area in several scalp regions. However, the morphometric evaluation of terminal anagen follicles demonstrated greater dimensions within the male group.

A infecção pelo vírus do herpes simples leva a um quadro clínico peculiar de fácil reconhecimento pelo médico. No entanto, em indivíduos imunossuprimidos, a apresentação clínica pode ser atípica, dificultando o diagnóstico e o tratamento. Em virtude disso, apresenta-se um caso de herpes simples ocorrendo em paciente submetido à quimioterapia.

The herpes simplex infection can produce peculiar clinical features easily recognized by the physician. However, in immunocompromised people, the clinical presentation can be atypical, difficulting the diagnosis and treatment. Therefore, a case of herpes simplex occurring in a pacient taking chemotherapy is presented.

Descreve-se uma família com síndrome dos cabelos anágenos frouxos (SCAF) associada à distrofia macular. Foram descritos os achados dermatológicos, oftalmológicos e de microscopia óptica e eletrônica de varredura de 11 indivíduos. Dois apresentaram SCAF, sem qualquer alteração ocular. Dos quatro indivíduos com alteração ocular, duas irmãs apresentaram SCAF e dispersões pigmentares em pólo posterior da retina, com coloboma da mácula. Em dois irmãos encontraram-se as mesmas características da SCAF e fundo de olho com dispersões pigmentares em pólo posterior, sem coloboma. Os achados sugerem que essa associação seja uma nova entidade nosológica dentro das displasias ectodérmicas.

The article describes a family with loose anagen hair syndrome (LAHS) associated with macular dystrophy. Complete dermatological and ophthalmological exams, and hair examination under optical and electron microscopy were performed in eleven index cases. Two individuals demonstrated hair findings with LAHS without ocular problems. Within the four cases with ocular problems, two sisters presented with LAHS and pigmentary dispersion on the retina with macular coloboma. Two brothers presented with LAHS and pigmentary dispersion on the retina without macular coloboma. The findings suggest that this new association is a disorder among the ectodermal dysplasia.