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4.
Indian Dermatol Online J ; 12(2): 312-315, 2021.
Artículo en Inglés | MEDLINE | ID: mdl-33959532

RESUMEN

Papular lesions over face have a wide range of differential diagnoses. The clinical differentiation among these is difficult and often requires clinicopathological correlation. We hereby report the case of a 28 year old female presenting with numerous skin colored papular lesions over face, pinna and upper limbs.

5.
Dermatol Online J ; 26(4)2020 Apr 15.
Artículo en Inglés | MEDLINE | ID: mdl-32621683

RESUMEN

Congenital atrichia with papular lesions is a rare, autosomal recessive and irreversible form of total alopecia of the body hair characterized by hair loss soon after birth and the development of keratinfilled cysts or horny papules over extensive areas of the body. The condition is associated with a mutation of the human hairless gene on chromosome region 8p12. We report a 1-year-old boy presenting with the absence of scalp and body hair since birth. On examination, he had complete absence of hair on the scalp, eyebrows, and eyelashes. Multiple, discrete, pearly-to-skin-colored papules of 1-3mm in size were present over the scalp. The skin biopsy from a scalp papule revealed normal overlying epidermis with multiple keratin cysts and hypoplastic hair follicles in the upper dermis.


Asunto(s)
Alopecia/congénito , Folículo Piloso/anomalías , Enfermedades Cutáneas Vesiculoampollosas/congénito , Piel/patología , Alopecia/diagnóstico , Alopecia/genética , Alopecia/patología , Biopsia , Consanguinidad , Diagnóstico Diferencial , Raquitismo Hipofosfatémico Familiar/diagnóstico , Folículo Piloso/patología , Humanos , Lactante , Masculino , Linaje , Enfermedades Cutáneas Vesiculoampollosas/diagnóstico , Enfermedades Cutáneas Vesiculoampollosas/genética , Enfermedades Cutáneas Vesiculoampollosas/patología
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