Results 31 to 40 of about 1,455,846 (152)

Kasabach-Merritt syndrome arising from an Enteroatmospheric Fistula [PDF]

, 2022
Kasabach-Merritt syndrome (KMS) is a rare, life-threatening condition that is characterized by profound thrombocytopenia, hypofibrinogenemia, elevated partial thromboplastin time, and may also be associated with microangiopathic hemolytic anemia.
Rajaratnam, Krishan, Shah, Kunal
core   +1 more source

Kaposiform hemangioendothelioma: radiological, surgical and anatomopathological correlation [PDF]

Revista Brasileira de Cirurgia Plástica, 2021
Introduction: Kaposiform cutaneous hemangioendothelioma (HEK) is a rare locally aggressive vascular tumor, seen mainly in newborns and children. It has a prevalence of 0.91 cases per 100,000 children, being most common in the extremities.
Katia Torres Batista, Hugo Jose de Araújo, Maria Ireni Zapalowski Galvão, Silvia Yumi Myasaki, Anna Luiza Galvão, Camila Freire Parente Alves da Silva   +5 more
doaj   +1 more source

Partially involuting congenital hemangioma with pyogenic granuloma‐induced rapid progression following incisional biopsy in infancy: A case report

Clinical Case Reports, Volume 11, Issue 10, October 2023., 2023
Clinical photographs illustrating the course of the congenital hemangioma in this case. Key Clinical Message We present a case of partially involuting congenital hemangioma (PICH) that showed rapid growth with ulceration after incisional biopsy. PICH does not typically grow after birth.
Yuki Sasaki, Kosuke Ishikawa, Takahiro Miura, Emi Funayama, Yuhei Yamamoto, Taku Maeda   +5 more
wiley   +1 more source

Spontaneous haemothorax as a complication of Kassabach‐Merritt phenomenon (KMP) in a‐2‐years old female child: A case report

Respirology Case Reports, Volume 11, Issue 10, October 2023., 2023
Kasabach‐Merritt phenomenon (KMP) is a rare condition that is associated with two rare vascular tumours: Kapossiform haemangioendothelioma (KHE) and tufted angioma (TA). We present the fatal case of a 2‐years girl diagnosed with KMP based on clinical, laboratory and imaging findings but died due to spontaneous rebleeding before biopsy could be ...
Citra Cesilia, Elmi Ridar, Hariadi Hatta, Andreas Makmur, FW Wiwit Ade, Heda Melinda Nataprawira   +5 more
wiley   +1 more source

Surgical treatment of kaposiform hemangioendothelioma in the pelvic cavity, bladder and ureter

Journal of Pediatric Surgery Case Reports, 2018
Kasabach-Merritt phenomenon (KMP) is a rare potentially life-threatening consumptive coagulopathy characterized by thrombocytopenia and hypofibrinogenemia occurring associated with the vascular tumors kaposiform hemangioendothelioma (KHE) and tufted ...
Li Xiao, Changxian Dong, Song Zuo, Yanlin Wang   +3 more
doaj   +1 more source

Large abdominal purpura of neonatal retroperitoneal kaposiform hemangioendothelioma

Clinical Case Reports, 2021
Large abdominal purpuras may be caused by retroperitoneal kaposiform hemangioendothelioma with consumptive coagulopathy. Clinicians should perform serial ultrasonography studies to detect the sings of tumor until the final diagnosis is confirmed.
Ryo Takemura, Yoshiro Wada
doaj   +1 more source

Surgical treatment of a huge kaposiform hemangioendothelioma in the chest wall: A case study

SAGE Open Medical Case Reports, 2016
Kaposiform hemangioendothelioma, a rare vascular pediatric tumor often associated with Kasabach–Merritt phenomenon, is characterized by severe thrombocytopenia and consumptive coagulopathy.
Xiaonan Guo, Yubin Gong, Changxian Dong
doaj   +1 more source

Kaposiform haemangioendothelioma with Kasabach-Merritt phenomenon, literature review

, 2022
Introducción: El hemangioendotelioma kaposiforme es un tumor vascular raro de crecimiento rápido, su principal complicación es el fenómeno de Kasabach-Merritt que se caracteriza por una trombocitopenia grave, coagulopatía por consumo y púrpura.
Medina López, Yuliana Montserrat, Sánchez Grijalva, Claudia Ivette, Campos Félix, Lucero Beatriz, García López, José Saúl, Calderón Alvarado, Ana Beatriz   +4 more
core   +1 more source

Japanese Clinical Practice Guidelines for Vascular Tumors, Vascular Malformations, Lymphatic Malformations, and Lymphangiomatosis 2022

The Journal of Dermatology, Volume 53, Issue 5, Page e257-e356, May 2026.
ABSTRACT The objective was to prepare guidelines to perform the current optimum treatment by organizing effective and efficient treatments of hemangiomas and vascular malformations, confirming the safety, and systematizing treatment, employing evidence‐based medicine techniques and aimed at improvement of the outcomes.
Yoshiaki Kinoshita, Kosuke Ishikawa, Sadanori Akita, Katsuyoshi Koh, Satoru Sasaki, Masatoshi Jinnin, Hidefumi Mimura, Keigo Osuga, Michio Ozeki, Michiko Nagahama, Akihiro Fujino, Yoko Aoki, Akiko Asai, Noriko Aramaki‐Hattori, Ryohei Ishiura, Masanori Inoue, Yuki Iwashina, Takafumi Ohshiro, Keiko Ogawa, Mine Ozaki, Junko Ochi, Shiro Onozawa, Motoi Kato, Takahide Kaneko, Tamihiro Kawakami, Akira Kitagawa, Masakazu Kurita, Yoshihiro Kuwano, Taro Kono, Shien Seike, Shinsuke Takagi, Nobuyuki Takakura, Takao Tachibana, Shuichi Tanoue, Kumiko Chuman, Hiroki Nakaoka, Yasuhiro Nakamura, Fumio Nagai, Yasunari Niimi, Shunsuke Nosaka, Taiki Nozaki, Tadashi Nomura, Kazuki Hashimoto, Ayato Hayashi, Satoshi Hirakawa, Takeshi Hirabayashi, Taizo Furukawa, Hiroshi Furukawa, Yumiko Hori, Takanobu Maekawa, Kentaro Matsuoka, Hideki Mori, Eiichi Morii, Akira Morimoto, Yuta Moriwaki, Shunsuke Yuzuriha, Naoaki Rikihisa, Munezumi Fujita, Yasuyuki Yamahana, Kyoichi Deie, Asami Tozawa, Daisuke Hasegawa, Akira Higashiyama, Daisuke Maeda, Sachiko Asayama, Yuhki Arai, Yohei Iwata, Mayu Uka, Hidehito Usui, Mizuki Uchiyama, Saori Endo, Hideki Endo, Rintaro Ono, Naoya Oshima, Toshihiro Otsuka, Kuniaki Ohara, Shinji Kagami, Tomo Kakihara, Mototoshi Kato, Hiroki Kanamori, Masafumi Kamata, Ami Kawaguchi, Akiko Kishi, Hiroshi Kitagawa, Kiyokazu Kim, Tamotsu Kobayashi, Takeshi Saito, Yusuke Shikano, Shuichi Shimada, Keisuke Suzuki, Masataka Takahashi, Shohei Takami, Reiko Takeda, Aya Tanaka, Kaishu Tanaka, Satoru Tamura, Masashi Tamura, Kanako Danno, Kenji Tsuboi, Yuta Nakajima, Ryo Nakatani, Miho Noguchi, Akifumi Nozawa, Naoki Hashizume, Masashi Hayakawa, Daichi Hayashi, Takaya Fukumoto, Mamoru Honda, Norifumi Matsuda, Hayato Maruguchi, Naoki Murakami, Kiichiro Yaguchi, Shiho Yasue, Hiroki Yoshihara, Rika Yoshimatsu, Kiyohito Yamamoto, Shinji Wada   +116 more
wiley   +2 more sources

Impact of sirolimus treatment for refractory kaposiform hemangioendothelioma with exacerbation of the disease 10 years after initial diagnosis

Rare Tumors, 2018
We describe our experience with a 12 year-old girl with kaposiform hemangioendothelioma accompanied by Kasabach–Merritt phenomenon with exacerbation of the disease 10 years after the initial diagnosis. Kaposiform hemangioendothelioma infiltrated into the
Naoki Sakata, So-ichi Suenobu, Munehiro Okano, Satoshi Ueda, Masatomo Kimura, Tsukasa Takemura   +5 more
doaj   +1 more source