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出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2014/06/02 02:52:08」(JST)

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1. 房状血管腫、カポジ肉腫様血管腫、およびKasabach‐Merritt現象 tufted angioma kaposiform hemangioendothelioma and the kasabach merritt phenomenon
2. 幼児血管腫の評価および診断 evaluation and diagnosis of infantile hemangiomas
3. 先天性血管腫：急速退縮性先天性血管腫（RICH）および非退縮性先天性血管腫（NICH） congenital hemangiomas rapidly involuting congenital hemangioma rich and noninvoluting congenital hemangioma nich
4. 幼児血管腫の疫学、病因、臨床的特徴、および合併症 epidemiology pathogenesis clinical features and complications of infantile hemangiomas
5. 小児における皮膚蒼白の評価 evaluation of pallor in children

Adult-onset tufted angiomas associated with an arteriovenous malformation in a renal transplant recipient: case report and review of the literature.

Grassi S1, Carugno A, Vignini M, Rosso R, Borroni RG.
The American Journal of dermatopathology.Am J Dermatopathol.2015 Feb;37(2):162-5. doi: 10.1097/DAD.0000000000000221.
: Tufted angioma (TA) is a rare benign vascular neoplasm characterized histopathologically by the proliferation of endothelial cells arranged in lobules in the dermis and subcutaneous fat. To date, about 200 cases have been reported, most of which are of Japanese ethnicity. TA predominantly affects
PMID 25365496

The importance of early diagnosis and treatment of kaposiform hemangioendothelioma complicated by Kasabach-Merritt phenomenon.

Vivas-Colmenares GV1, Ramirez-Villar GL2, Bernabeu-Wittel J3, Matute de Cardenas JA1, Fernandez-Pineda I1.
Dermatology practical & conceptual.Dermatol Pract Concept.2015 Jan 30;5(1):91-3. doi: 10.5826/dpc.050118. eCollection 2015.
Kaposiform hemangioendothelioma (KHE) is a locally aggressive vascular tumor that may be complicated by Kasabach-Merritt phenomenon (KMP), a profound thrombocytopenia resulting from platelet trapping within a vascular tumor, either KHE or tufted angioma (TA). Typical features also include low fibrin
PMID 25692091

Yamamoto Y1, Kounami S, Okuhira H, Nakamura Y, Furukawa F.
The Journal of dermatology.J Dermatol.2014 Dec;41(12):1120-2. doi: 10.1111/1346-8138.12665. Epub 2014 Nov 11.
PMID 25388632