RESUMO
Satoyoshi syndrome is a rare multisystemic disorder characterized by alopecia, diarrhea, muscle spasms, osseous abnormalities, and endocrinopathies. We report a case of Satoyoshi syndrome misdiagnosed as vitamin D-dependent rickets for several years.
Assuntos
Alopecia/complicações , Alopecia/etiologia , Alopecia/patologia , Osso e Ossos/anormalidades , Diarreia/complicações , Diarreia/patologia , Espasmo/complicações , Espasmo/patologia , Alopecia/diagnóstico por imagem , Osso e Ossos/diagnóstico por imagem , Osso e Ossos/patologia , Criança , Erros de Diagnóstico , Diarreia/diagnóstico por imagem , Feminino , Humanos , Osteólise/diagnóstico por imagem , Osteólise/etiologia , Radiografia , Pele/patologia , Espasmo/diagnóstico por imagemRESUMO
Eccrine spiradenoma (ES) is a benign uncommon tumor of skin adnexa with a characteristic clinical and histopathological presentation. Typically, it presents as a painful, slow growing and solitary nodule on the head or upper trunk in adult patients. We report a child with linear ES which presented with asymptomatic papulonodular lesions in a blaschkoid distribution on the face. Cases reported in the literature of multiple spiradenomas are very rare and multiple linear lesions are even rarer. To date, 21 cases of linear/multiple ES have been reported. Of these, eight were in children or adolescents. We report an additional case of this rare clinical presentation and review the literature.
Assuntos
Adenoma de Glândula Sudorípara/congênito , Glândulas Écrinas/patologia , Neoplasias Primárias Múltiplas/congênito , Neoplasias das Glândulas Sudoríparas/congênito , Adenoma de Glândula Sudorípara/patologia , Criança , Feminino , Humanos , Neoplasias Primárias Múltiplas/patologia , Neoplasias das Glândulas Sudoríparas/patologiaAssuntos
Ambulatório Hospitalar , Dermatopatias/epidemiologia , Adulto , Estudos Transversais , Serviços Médicos de Emergência , Feminino , Humanos , Ceratose Seborreica/diagnóstico , Ceratose Seborreica/epidemiologia , Ceratose Seborreica/terapia , Masculino , Dermatopatias/diagnóstico , Dermatopatias/terapia , Espanha/epidemiologiaAssuntos
Anticolesterolemiantes/administração & dosagem , Colesterol/administração & dosagem , Ictiose/tratamento farmacológico , Lovastatina/administração & dosagem , Nevo/tratamento farmacológico , Síndrome de Sjogren-Larsson/tratamento farmacológico , Neoplasias Cutâneas/tratamento farmacológico , Adulto , Quimioterapia Combinada , Feminino , Humanos , Nevo/patologia , Síndrome de Sjogren-Larsson/patologia , Neoplasias Cutâneas/patologia , Adulto JovemAssuntos
Dermatite Perioral/tratamento farmacológico , Fármacos Dermatológicos/administração & dosagem , Tacrolimo/análogos & derivados , Administração Tópica , Adulto , Dermatite Perioral/patologia , Fármacos Dermatológicos/uso terapêutico , Humanos , Masculino , Tacrolimo/administração & dosagem , Tacrolimo/uso terapêutico , Fatores de Tempo , Resultado do TratamentoRESUMO
Dyschromatosis universalis hereditaria (DUH) is a rare genodermatosis mainly described in asian subjects. Here, we report a case of a caucasian 11-year-old boy with DUH and an unaffected twin brother. Parents were not consanguineous. A review of the main phenotical, clinical and hystological aspects of this rare entity is exhibited. Differential diagnose might be stablished with several pigmentary disorders, so Dermatologist might have this entity in mind to make a correct diagnose, specially in cases with no response to typical treatments.
RESUMO
Mantle cell lymphoma is a type of non-Hodgkin lymphoma that affects extranodal areas, especially, bone narrow, digestive tract and Waldeyer ring. Here we report a case of mantle cell lymphoma IV Ann Arbor stage with cutaneous lesions on nasal dorsum and glans penis as the first manifestations. Skin involvement is a very rare manifestation and less than 20 cases have been reported in the literature. The importance of establishing multidisciplinary relationships for a global approach has been shown by this clinical case.
RESUMO
A variety of tumors develop or exacerbate during pregnancy and it is well known that a noticeable increase of eccrine activity occurs in this period. Eccrine poroma is a benign neoplasm that originates from the eccrine sweat gland. The development of this tumor during pregnancy is extremely infrequent. We report a rare case of rapidly growing eccrine poroma in an unusual location (the nose) in a pregnant woman.