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Diffuse Capillary Malformation With Overgrowth (DCMO): A Case Report and Literature Review.
Fageeh, Sarah M; Alhothali, Omar S; Alharbi, Sara F; Alsaedi, Ethar T; Alsulami, Rola R; Alharbi, Ahmad N; Alamri, Ghadeer E; Al Hawsawi, Khalid.
Afiliación
  • Fageeh SM; Medicine and Surgery, Umm Al-Qura University, Makkah, SAU.
  • Alhothali OS; Medicine and Surgery, Umm Al-Qura University, Makkah, SAU.
  • Alharbi SF; Medicine and Surgery, Umm Al-Qura University, Makkah, SAU.
  • Alsaedi ET; Medicine and Surgery, Umm Al-Qura University, Makkah, SAU.
  • Alsulami RR; Medicine and Surgery, Umm Al-Qura University, Makkah, SAU.
  • Alharbi AN; Department of Dermatology, Taibah University, Medina, SAU.
  • Alamri GE; Medicine and Surgery, Umm Al-Qura University, Makkah, SAU.
  • Al Hawsawi K; Dermatology, King Abdulaziz Hospital Makkah, Makkah, SAU.
Cureus ; 15(3): e35776, 2023 Mar.
Article en En | MEDLINE | ID: mdl-37025729
ABSTRACT
Diffuse capillary malformation with overgrowth (DCMO) is a rare condition that is characterized by capillary malformation and soft tissue hypertrophy. Here we report the case of a one-year-old male child with no past medical history who presented with skin lesions persistent since birth and associated with no symptoms. There were widespread non-scaly reticulated erythematous patches all over his body, including the abdominal wall. The circumference of the right calf and mid-thigh was 13 cm and 20 cm respectively whereas the circumference of the left calf and mid-thigh was 11 cm and 18 cm respectively. The length of both lower extremities was similar. There was also syndactyly of the right second and third toes. Differential diagnoses include cutis marmorata telangiectatica congenita (CMTC), DCMO, and macrocephaly-capillary malformation (M-CM) syndrome. Based on clinical features, the patient was diagnosed with DCMO. He was put under follow-up by pediatric orthopedics for periodic monitoring of growth asymmetry.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Cureus Año: 2023 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Cureus Año: 2023 Tipo del documento: Article