Results 21 to 30 of about 900 (120)

Kasabach–Merritt phenomenon

Indian Journal of Paediatric Dermatology, 2019
Kasabach-Merritt Phenomenon (KMP) is a potentially life-threatening condition characterised by thrombocytopenic consumptive coagulopathy. KMP is almost exclusively associated with two uncommon vascular tumours, Kaposiform haemangioendotheliomas (KHE) and
Sanjay Singh, Neetu Bhari, Rubina Jassi
doaj   +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

Neonatal Kasabach-Merritt phenomenon

Indian Journal of Medical and Paediatric Oncology, 2011
Kasabach-Merritt phenomenon (KMP) is a life-threatening consumptive coagulopathy in the presence of a rapidly enlarging vascular tumor. It usually presents in early infancy, but onset in early neonatal period, facial hemangioma, and vincristine use in ...
Dinesh Yadav, Anu Maheshwari, Satinder Aneja, Anju Seth, Jagdish Chandra   +4 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

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

Prenatal detection of Kaposiform Hemangioendothelioma with Kasabach–Merritt phenomenon: a case report

The Egyptian Journal of Radiology and Nuclear Medicine, 2023
Background Kaposiform Hemangioendothelioma is a rare vascular neoplasm that typically presents in neonates and infancy. Most of the cases of Kaposiform Hemangioendothelioma are reported in neonates (60%) and infancy (93%), and very few cases have been ...
Vinay Maurya, Shweta Sharma, Samarjeet Singh, Pankaj Sharma, Amul Gupta   +4 more
doaj   +1 more source