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A case of mediastinal kaposiform hemangioendothelioma complicated with Kasabach-Merritt syndrome

2023; Volume: 13; Issue: 1 Linguagem: Inglês

10.25060/residpediatr-2023.v13n1-479

2236-6814

Luanna Novais, Alef Vieira, B Rocha, Erika Correia, Braulio Silva Neto, Breno Wanderley, Amanda Machado, Mila Alves,

Cardiac tumors and thrombi

OBJECTIVES: This paper reports the case of a child diagnosed with mediastinal kaposiform hemangioendothelioma (KHE) and Kasabach-Merritt Syndrome at a referral hospital in Salvador, Bahia, Brazil. CASE REPORT: A two-month-old with a history of cyanosis and nasal congestion had an echocardiogram with findings consistent with pericardial effusion. The patient underwent multiple pericardial drainage procedures and was eventually sent to a pediatric referral center in the city of Salvador. Contrast-enhanced computed tomography images showed a mediastinal mass, which was resected. Postoperative pathology revealed the patient had a KHE. He was also suspected with Kasabach-Merritt syndrome due to consumption coagulopathy. Corticoid therapy and chemotherapy with vincristine were performed. The patient progressed well and was discharged and placed on outpatient follow-up, without recurrence of symptoms. COMMENTS: KHE is rare and aggressive, although with a benign histopathology. It can complicate with consumption coagulopathy, characteristically seen in Kasabach-Merritt syndrome.