Acral porokeratosis associated with anonychia
نویسندگان
چکیده
منابع مشابه
Linear scleroderma with partial anonychia
Morphine inhibits the expression of antigenic markers for T-helper cells and also the respiratory burst of these cells.[6] This drug suppresses antibody production in response to the T cell-dependent antigens.[6] It also leads to elevated plasma levels of corticotropinreleasing hormone (CRH), adrenocorticotropic hormone (ACTH) and glucocorticoids.[6] Therefore, through suppression of the immune...
متن کاملEruptive disseminated porokeratosis associated with corticosteroid-induced immunosuppression.
Eruptive disseminated porokeratosis (EDP) is a disease that presents clinically with sudden onset of erythematous papules and plaques, with a ridge-like border histologically represented by a cornoid lamella. We report a case of EDP occurring in a 39-year-old woman 3 days after completion of a 2-week course of oral corticosteroid therapy for an acute asthma exacerbation. The patient was treated...
متن کاملAcral-type Malignant Acanthosis Nigricans Associated with Gastric Adenocarcinoma
Acanthosis nigricans is a symmetric eruption characterized by the presence of a hyperpigmented, velvety cutaneous thickening, that can develop on any part of the body, but characteristically affects the flexural areas of the body. The velvety hyperkeratotic lesions can be located on the dorsum of the hands and feet in dark-skinned people in the form of a variant of acanthosis nigricans called a...
متن کاملAmelanotic Acral Melanoma Associated with KIT Mutation and Vitiligo
Amelanotic acral melanoma is rare and difficult to diagnose, both clinically and pathologically. KIT mutations are frequently found in acral melanomas and are considered a risk factor for poor prognosis. The presence of vitiligo in melanoma has been reported, and KIT is thought to be partly responsible for the dysfunction and loss of melanocytes observed in vitiligo. We report a case of amelano...
متن کاملCongenital non-syndromic anonychia totalis with acroosteolysis.
Mian A, Jorwal P. BMJ Case Rep 2017. doi:10.1136/bcr-2017-222743 Description A 15-year-old boy presented with a history of absence of fingernails and toenails since birth. He was the first born of a non-consanguineous marriage, delivered vaginally at term with normal birth weight. His mother admitted to excessive consumption of opioid analgesics (ethyl morphine derivatives) during all three tri...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: Indian Journal of Dermatology, Venereology and Leprology
سال: 2018
ISSN: 0378-6323
DOI: 10.4103/ijdvl.ijdvl_940_16