Anetoderma of Jadassohn

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Nevus Sebaceus of Jadassohn

Figure 1. Hairless scalp vertex lesion present since birth that has been slowly enlarging.

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Cerebriform nevus sebaceous of Jadassohn.

An 11-year-old boy presented with raised pigmented lesion over the scalp since 10 years. Parents gave history of hairless yellowish plaque present over the scalp at birth which gradually increased to present size to take cerebriform appearance. There was no history of trauma. All routine hematological investigations were normal. No systemic and developmental defect was noted. X-ray skull, eye a...

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CT of sebaceous nevus syndrome (Jadassohn disease).

The sebaceous nevus, a congenital sk in disease, was first described in 1895 by Jadassohn [1] and later became known as the organoid nevus syndrome within the grouping of the phacomatoses [2]. In 1957 , Schimmelpenning [3] described its assoc iation with central nervous system, skeletal, and eye lesions. In 1962, Feuerstein and Mims [4] reported a case with epi lepsy and mental retardation . In...

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Primary anetoderma and antiphospholipid antibodies

Anetoderma is an elastolytic skin process clinically characterized by circumscribed rounded areas of loose skin; and histologically, by loss of elastic dermal fi bers. Two forms are traditionally distinguished, primary and secondary. Th e latter refers to an abnormal repair mechanism of preexisting skin lesions, where acne and varicella are the most frequent causes. In contrast, in the primary ...

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Secondary anetoderma associated with mastocytosis.

BACKGROUND Mastocytosis represents a wide spectrum of proliferative disorders of mast cells in the bone marrow, skin and/or internal organs. The most common manifestation is urticaria pigmentosa (UP), which is characterized by small or large brown-red maculopapules on the skin. Occasionally, elastic and collagen fibers in the lesions degenerate and result in a lax area of skin termed anetoderma...

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ژورنال

عنوان ژورنال: Journal of the Royal Society of Medicine

سال: 1988

ISSN: 0141-0768,1758-1095

DOI: 10.1177/014107688808101220