Linear and whorled nevoid hypermelanosis: A case report with dermoscopic findings
نویسندگان
چکیده
منابع مشابه
Linear and whorled nevoid hypermelanosis with hemiatrophy.
FIG. 1 Linear and Whorled Nevoid Hypermelanosis: Linear and whorled hyperpigmented macules in a reticulate pattern along the Blaschko’s lines over trunk and limbs. A two-years-old boy presented with abnormal body pigmentation and body asymmetry noted since birth. A preceding vesicular eruption was absent. He was developmentally normal. Family history was insignificant. Examination revealed line...
متن کاملLinear and whorled nevoid hypermelanosis in three successive generations.
Sir, Linear and whorled nevoid hypermelanosis (LWNH) is characterized by hyperpigmented macules in a streaky configuration along the lines of Blaschko, without preceding inflammation or atrophy.[1-3] Lesions are distributed mainly on the trunk and extremities, sparing palms, soles, and mucosae. The usual age of the onset of hyperpigmentation occurs within the first few weeks of life, continues ...
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Observations: Porokeratosis is a dyskeratotic disorder of the skin characterized by hyperkeratotic papule or plaque with an annular appearance and usually diagnosed easily, both histopathologically and clinically. We present a case of linear porokeratosis which was most likely suggesting the linear epidermal nevus and linear lichen planus. We observed a tiny brown border in the dermoscopic exam...
متن کاملClinical and dermoscopic findings in Goltz syndrome: case report.
Focal dermal hypoplasia or Goltz syndrome is a rare X-linked genodermatosis characterized by cutaneous and musculoskeletal defects. Dermoscopy is a noninvasive auxiliary method for the diagnosis of lesions, whether melanocytic or not. Its widespread use in dermatology is resulting in the description of new patterns and characterization of lesions not reported before its use. A typical case of G...
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ژورنال
عنوان ژورنال: Indian Journal of Dermatology, Venereology, and Leprology
سال: 2016
ISSN: 0378-6323
DOI: 10.4103/0378-6323.171007