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A Huge Subcutaneous Hematoma in an Adult with Kasabach-Merritt Syndrome

Patient: Male, 1 Final Diagnosis: Kasabach-Merritt syndrome with widespread hemangiomas and an infected huge hematoma in the right thigh Symptoms: Gross hematuria Medication: — Clinical Procedure: CT-guided drainage • blood transfusion Specialty: Hematology OBJECTIVE: Rare disease BACKGROUND: Kasaba...

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Autores principales: Wu, Kuan-Lin, Liao, Chiung-Ying, Chang, Chen-Kuang, Ho, Shang-Yun, Tyan, Yeu-Sheng, Huang, Yuan-Chun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Scientific Literature, Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5484458/
https://www.ncbi.nlm.nih.gov/pubmed/28626212
http://dx.doi.org/10.12659/AJCR.901947
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author Wu, Kuan-Lin
Liao, Chiung-Ying
Chang, Chen-Kuang
Ho, Shang-Yun
Tyan, Yeu-Sheng
Huang, Yuan-Chun
author_facet Wu, Kuan-Lin
Liao, Chiung-Ying
Chang, Chen-Kuang
Ho, Shang-Yun
Tyan, Yeu-Sheng
Huang, Yuan-Chun
author_sort Wu, Kuan-Lin
collection PubMed
description Patient: Male, 1 Final Diagnosis: Kasabach-Merritt syndrome with widespread hemangiomas and an infected huge hematoma in the right thigh Symptoms: Gross hematuria Medication: — Clinical Procedure: CT-guided drainage • blood transfusion Specialty: Hematology OBJECTIVE: Rare disease 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.
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spelling pubmed-54844582017-07-05 A Huge Subcutaneous Hematoma in an Adult with Kasabach-Merritt Syndrome Wu, Kuan-Lin Liao, Chiung-Ying Chang, Chen-Kuang Ho, Shang-Yun Tyan, Yeu-Sheng Huang, Yuan-Chun Am J Case Rep Articles Patient: Male, 1 Final Diagnosis: Kasabach-Merritt syndrome with widespread hemangiomas and an infected huge hematoma in the right thigh Symptoms: Gross hematuria Medication: — Clinical Procedure: CT-guided drainage • blood transfusion Specialty: Hematology OBJECTIVE: Rare disease 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. International Scientific Literature, Inc. 2017-06-19 /pmc/articles/PMC5484458/ /pubmed/28626212 http://dx.doi.org/10.12659/AJCR.901947 Text en © Am J Case Rep, 2017 This work is licensed under Creative Common Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) )
spellingShingle Articles
Wu, Kuan-Lin
Liao, Chiung-Ying
Chang, Chen-Kuang
Ho, Shang-Yun
Tyan, Yeu-Sheng
Huang, Yuan-Chun
A Huge Subcutaneous Hematoma in an Adult with Kasabach-Merritt Syndrome
title A Huge Subcutaneous Hematoma in an Adult with Kasabach-Merritt Syndrome
title_full A Huge Subcutaneous Hematoma in an Adult with Kasabach-Merritt Syndrome
title_fullStr A Huge Subcutaneous Hematoma in an Adult with Kasabach-Merritt Syndrome
title_full_unstemmed A Huge Subcutaneous Hematoma in an Adult with Kasabach-Merritt Syndrome
title_short A Huge Subcutaneous Hematoma in an Adult with Kasabach-Merritt Syndrome
title_sort huge subcutaneous hematoma in an adult with kasabach-merritt syndrome
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5484458/
https://www.ncbi.nlm.nih.gov/pubmed/28626212
http://dx.doi.org/10.12659/AJCR.901947
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