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Erschienen in: Wiener klinische Wochenschrift 11-12/2015

01.06.2015 | case report

Unusual treatment of Kasabach–Merritt syndrome secondary to hepatic hemangioma: embolization with bleomycin

verfasst von: MD Halil Bozkaya, MD Celal Cinar, MD Ömer Vedat Ünalp, MD Mustafa Parildar, MD Ismail Oran

Erschienen in: Wiener klinische Wochenschrift | Ausgabe 11-12/2015

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Summary

Kasabach–Merritt syndrome (KMS) is a rare complication of cavernous hemangiomas characterized with anemia, thrombocytopenia, and consumption coagulopathy. This syndrome usually develops due to superficial soft tissue hemangiomas in infancy and childhood. KMS developing secondarily to hepatic hemangioma is very rare. In this report, we aimed to present the treatment of KMS developing secondarily to giant cavernous hemangioma of the liver with transarterial chemoembolization using bleomycin
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Metadaten
Titel
Unusual treatment of Kasabach–Merritt syndrome secondary to hepatic hemangioma: embolization with bleomycin
verfasst von
MD Halil Bozkaya
MD Celal Cinar
MD Ömer Vedat Ünalp
MD Mustafa Parildar
MD Ismail Oran
Publikationsdatum
01.06.2015
Verlag
Springer Vienna
Erschienen in
Wiener klinische Wochenschrift / Ausgabe 11-12/2015
Print ISSN: 0043-5325
Elektronische ISSN: 1613-7671
DOI
https://doi.org/10.1007/s00508-014-0675-5