Literature DB >> 15916565

Nevus psiloliparus and aplasia cutis: a further possible example of didymosis.

Antonio Torrelo1, María del C Boente, Olga Nieto, Raúl Asial, Isabel Colmenero, Beatriz Winik, Antonio Zambrano, Rudolf Happle.   

Abstract

Nevus psiloliparus is a distinct type of mesodermal nevus of the scalp characterized by absence or paucity of hair, and presence of an excessive amount of fatty tissue. It is considered a hallmark of encephalocraniocutaneous lipomatosis, a rare disorder comprising a variety of cutaneous, ophthalmologic, and neurologic defects. We report two infants with encephalocraniocutaneous lipomatosis with nevus psiloliparus on the scalp in close association with aplasia cutis congenita. This unusual association may be considered a further example of didymosis, for which we propose the term, didymosis aplasticopsilolipara.

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Year:  2005        PMID: 15916565     DOI: 10.1111/j.1525-1470.2005.22305.x

Source DB:  PubMed          Journal:  Pediatr Dermatol        ISSN: 0736-8046            Impact factor:   1.588


  3 in total

1.  Multiple aplasia cutis congenita lesions located along Blaschko's lines in a patient with tetralogy of Fallot-A.

Authors:  Daiki Rokunohe; Eijiro Akasaka; Akiko Rokunohe; Takahide Kaneko; Yasushi Matsuzaki; Noriko Takiyoshi; Takayuki Aizu; Hajime Nakano; Daisuke Sawamura
Journal:  J Dermatol Case Rep       Date:  2012-06-30

2.  Giant Ocular Lipodermoid Cyst in Encephalocraniocutaneous Lipomatosis: Surgical Treatment and Genetic Analysis.

Authors:  Andrea Córdoba; Enrique O Graue-Hernández; Alejandro Navas; Oscar F Chacon-Camacho; Juan C Zenteno; Arturo Ramirez-Miranda; Jose Antonio Bermudez-Magner; Thania Ordaz-Robles; Sofia Pérez-Solórzano; Andrew Olivo-Payne
Journal:  Am J Case Rep       Date:  2019-10-25

3.  Encephalocraniocutaneous lipomatosis (Haberland syndrome): A mild case with bilateral cutaneous and ocular involvement.

Authors:  Jonathan Banta; Knox Beasley; Todd Kobayashi; Luis Rohena
Journal:  JAAD Case Rep       Date:  2016-04-15
  3 in total

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