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1.
Clin Case Rep ; 10(10): e6443, 2022 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-36245467

RESUMEN

Omphalolith is a rare and underdiagnosed entity due to the accumulation of sebum and keratin in the umbilicus. It usually occurs in the elderly with deep and narrow umbilicus. Early recognition of omphalolith is important to prevent complications, unnecessary investigations, and anxiety. We report herein two new cases of omphalolith.

3.
Clin Dermatol ; 40(4): 388-394, 2022.
Artículo en Inglés | MEDLINE | ID: mdl-35181410

RESUMEN

Autosomal recessive congenital ichthyosis (ARCI) is a clinically and genetically heterogeneous category of nonsyndromic ichthyosis. Nail changes in ARCI are generally frequent but have been rarely reported and studied in the literature. This stimulated us to conduct a study to describe nail changes in ARCI using a combined literature review and prospective examination from March 2019 to August 2019 (6 months) in the Dermatology Department of Habib Thameur Hospital, Tunis, Tunisia. A total of 25 patients with ARCI had a clinical and dermatoscopic review. The mean age was 19.8 years (range, 1-43), with a female predominance (17 women [68%] and 8 men [32%]). Seventy-two percent had nail unit changes involving more than one nail, none had single nail disease, 64% had involvement of fingernails, and 68% had involvement of toenails, with cases including periungual hyperkeratosis (64%), xanthonychia (40%), pachyonychia (40%), macrolunula (36%), digital clubbing (32%), and onychomycosis (24%). Rarer findings included pseudoainhum, transverse leukonychia, longitudinal melanonychia, and subungual hemorrhages, each in one patient (4%). There was a statistically significant increased frequency of nail changes in adults over children (P = .001). Nail abnormalities statistically associated with ARCI were macrolunula, periungual hyperkeratosis, xanthonychia, and pachyonychia. A comprehensive review of the literature was performed, creating the first comprehensive review addressing nail disease in ARCI.


Asunto(s)
Ictiosis Lamelar , Ictiosis , Enfermedades de la Uña , Uñas Malformadas , Adulto , Niño , Femenino , Humanos , Ictiosis/diagnóstico , Ictiosis Lamelar/diagnóstico , Masculino , Enfermedades de la Uña/genética , Uñas , Uñas Malformadas/genética , Estudios Prospectivos , Adulto Joven
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