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Facial cleft presenting as a congenital facial papule.
Gao, Julia L; Rogers, Gary F; Myseros, John S; Habeshian, Kaiane A.
Afiliação
  • Gao JL; George Washington University School of Medicine and Health Sciences, Washington, District of Columbia, United States.
  • Rogers GF; George Washington University School of Medicine and Health Sciences, Washington, District of Columbia, United States.
  • Myseros JS; Division of Plastic Surgery, Children's National Health System, Washington, District of Columbia, United States.
  • Habeshian KA; George Washington University School of Medicine and Health Sciences, Washington, District of Columbia, United States.
Pediatr Dermatol ; 39(6): 990-991, 2022 Nov.
Article em En | MEDLINE | ID: mdl-35677994
ABSTRACT
Tessier number 3 craniofacial clefts are a rare congenital deformity of the oronasoocular region with variable severity, most often with serious impacts on appearance and function due to involvement of the bone and soft tissue. However, they can occasionally manifest mildly as a skin-colored congenital facial papule present with subtle anatomic anomalies and signs of deeper involvement, such as crusting and oozing. Recognizing that a congenital facial papule, including non-midline lesions, may be the presenting sign of an underlying developmental anomaly is important to avoid missing the diagnosis of a more extensive underlying congenital defect. We present a rare case of a forme fruste variant of a Tessier number 3 craniofacial cleft to raise awareness of its presentation and advise initial management in hopes of improving outcomes.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Anormalidades da Pele / Anormalidades Craniofaciais Tipo de estudo: Diagnostic_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Anormalidades da Pele / Anormalidades Craniofaciais Tipo de estudo: Diagnostic_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article