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A rare case of Kasabach Merritt Syndrome presenting with an infantile hemangioma: A case report.
Alghobaishi, Abdullah; Mousa, Ahmed Hafez; Almonaye, Haleema Sami; Maghrebi, Tasneem Khalid; Baothman, Abdullah; Al Shareef, Fawaz.
Afiliação
  • Alghobaishi A; Department of Pediatrics, Pediatrics Critical Care Medicine, King Fahad Armed Forces Hospital, Jeddah, Saudi Arabia.
  • Mousa AH; Department of Pediatrics, Saudi German Hospital, Jeddah, Saudi Arabia.
  • Almonaye HS; Department of Medicine and Surgery, Batterjee Medical College, Jeddah, Saudi Arabia.
  • Maghrebi TK; Department of Pediatrics, Saudi German Hospital, Jeddah, Saudi Arabia.
  • Baothman A; Department of Medicine and Surgery, Batterjee Medical College, Jeddah, Saudi Arabia.
  • Al Shareef F; Department of Pediatrics, Saudi German Hospital, Jeddah, Saudi Arabia.
Ann Med Surg (Lond) ; 76: 103557, 2022 Apr.
Article em En | MEDLINE | ID: mdl-35495392
Introduction: and importance: Infantile hemangioma, being a benign tumor of the blood vessel, is part of a triad composed of also thrombocytopenia and hypofibrinogenemia as part of Kasabach Merrit Syndrome. Case presentation: We report the case of a 2 months old female Saudi infant referred due to respiratory distress, thrombocytopenia, and enlarging hemangioma on right upper chest, neck, and lower cheek. Diagnosis of kaposiform hemangioendothelioma complicated by Kasabach Merritt thrombocytopenia was done based on the clinical triad of thrombocytopenia, bleeding tendency, and the presence of a vascular tumor. Conclusion: Vincristine and CTA embolization are lines of management that showed to be the most efficient in the improvement of the clinical picture of KMS in our patient.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article