19 June 2017
: Case report
A Huge Subcutaneous Hematoma in an Adult with Kasabach-Merritt Syndrome
Rare disease
Kuan-Lin Wu1E, Chiung-Ying Liao1E, Chen-Kuang Chang2B, Shang-Yun Ho1D, Yeu-Sheng Tyan34F, Yuan-Chun Huang134ABEF*DOI: 10.12659/AJCR.901947
Am J Case Rep 2017; 18:682-686
Abstract
BACKGROUND: Kasabach-Merritt syndrome is a potentially fatal disease that consists of hemangioma(s) with thrombocytopenia, microangiopathic hemolytic anemia, and coagulopathy. Extensive hemangiomatosis is rare. We present the radiological features and treatment strategy of a young adult suffering from Kasabach-Merritt syndrome with widespread hemangiomas and an infected huge hematoma in the right thigh.
CASE REPORT: A 33-year-old Taiwanese male presented with a painful 20-cm mass over his right thigh and gross hematuria for 2 days. Hemangiomatosis was bioptically proven in infancy and the patient was under regular follow-up. Physical examination revealed normal heart rate, respiratory rate, and body temperature. Multiple palpable lumps with brown and purple areas of skin over the neck, trunk, and right thigh were noted. Laboratory examinations revealed thrombocytopenia anemia and elevated fibrin degradation products. There were no signs of sepsis. Blood transfusion and steroid therapy were executed. Computed tomography showed a huge complicated subcutaneous hematoma in the right thigh. Drainage of the huge hematoma was performed and antibiotics were prescribed. After the local infection in the right thigh and the bleeding tendency were controlled, the patient was discharged in a stable condition two weeks later.
CONCLUSIONS: A huge infected hematoma and widespread hemangiomas are extremely rare complications of Kasabach-Merritt syndrome. There are no known treatment guidelines currently available. Our patient was successfully treated with steroids, drainage, and antibiotics.
Keywords: Hematoma, Kasabach-Merritt syndrome, Thrombocytopenia
In Press
Case report
Am J Case Rep In Press; DOI: 10.12659/AJCR.945921
Case report
Am J Case Rep In Press; DOI: 10.12659/AJCR.946916
Case report
Am J Case Rep In Press; DOI: 10.12659/AJCR.946269
Case report
Am J Case Rep In Press; DOI: 10.12659/AJCR.948017
Most Viewed Current Articles
21 Jun 2024 : Case report
93,397
DOI :10.12659/AJCR.944371
Am J Case Rep 2024; 25:e944371
07 Mar 2024 : Case report
51,131
DOI :10.12659/AJCR.943133
Am J Case Rep 2024; 25:e943133
20 Nov 2023 : Case report
27,838
DOI :10.12659/AJCR.941424
Am J Case Rep 2023; 24:e941424
18 Feb 2024 : Case report
22,970
DOI :10.12659/AJCR.943030
Am J Case Rep 2024; 25:e943030