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Wiener klinische Wochenschrift
Erschienen in:

01.06.2015 | case report

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

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

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
Vorheriger Artikel Konsekutive Umstellung auf Tapentadol PR verbessert Analgesie und Lebensqualität bei Patienten mit starken und chronischen Schmerzen unter Tramadol > 300 mg/d
Nächster Artikel Ectopic acromegaly due to a growth hormone-secreting neuroendocrine-differentiated tumor developed from ovarian mature cystic teratoma
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Metadaten
Titel
Unusual treatment of Kasabach–Merritt syndrome secondary to hepatic hemangioma: embolization with bleomycin
verfasst von
Halil Bozkaya, MD
Celal Cinar, MD
Ömer Vedat Ünalp, MD
Mustafa Parildar, MD
Ismail Oran, MD
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

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