Results 61 to 70 of about 3,079 (142)

Neonatal kaposiform hemangioendothelioma of the spleen associated with Kasabach-Merritt phenomenon

, 2016
Kaposiform hemangioendothelioma is a rare locally aggressive vascular tumor that usually manifests during early childhood. Typically the lesion presents with skin, soft tissue and bone involvement and is characterized histologically by ill-defined ...
Shabtaie, Samuel A, Corrales-Medina, Fernando F, Infante, Juan C, Owyong, Mark, Ruiz-Mesa, Catalina, Rojas, Claudia P, Perez, Eduardo A, Sola, Juan E, Hogan, Anthony R, Wang, Bo, Neville, Holly L   +10 more
core   +1 more source

Differential Expression of ERG, CD31, CD34, and D2‐40 in Representative Vascular Tumors and Lymphatic Malformation‐Associated Lesions‐A Retrospective Study

Dermatologic Therapy, Volume 2026, Issue 1, 2026.
The distinction between vascular anomalies is clinically challenging due to their similar clinical presentations and pathological features. This study assessed the immunohistochemical expression of ERG, CD31, CD34, and D2‐40 in representative vascular tumors and lymphatic malformation‐associated lesions to evaluate their diagnostic value and inform ...
Lurun Wang, Chao Ji, Bo Cheng, Ziping Zhang, Jinwen Huang, Xianhui Wang   +5 more
wiley   +1 more source

Digitizing Diagnoses: Distinguishing Infantile Hemangiomas From Other Vascular Anomalies

Pediatric Dermatology, Volume 42, Issue 5, Page 998-1003, September/October 2025.
ABSTRACT Background/Objectives Generative artificial intelligence (AI) models have become increasingly accessible and advanced with multimodal input. Infantile hemangiomas (IHs) are the most common pediatric vascular tumor, but pediatricians may have difficulty distinguishing them from similar‐appearing lesions.
Aretha On, Elena Huang, Jessica Hills, Jared Pasternak, Joanne Alfandre, Griffin Stockton Hogrogian, Albert C. Yan   +6 more
wiley   +1 more source

Massive Congenital Vascular Tumor of Lower Limb: Kaposiform Hemangioendothelioma

, 2018
We report a neonate with congenital Kaposiform hemangioendothelioma of left thigh and diagnostic dilemmas encountered in the management. The lesion was dealt with en-bloc resection in early infancy which was proven curative.
Parveen Kumar, Yogesh Kumar Sarin
core   +1 more source

Kaposiform hemangioendothelioma causing intestinal obstruction

Journal of Pediatric Surgery Case Reports, 2018
A previously healthy toddler with bilious vomiting and erythematous gluteal rash over 2 weeks had intermittent pain, constipation and decreased appetite. All labs were negative with the exception of fecal occult blood.
Bassel Salman, Jatin Sharma, Austen Knapp, Begum Akay, Donald Gibson   +4 more
doaj   +1 more source

Kaposiform hemangioendothelioma with Kasabach–Merritt phenomenon in a neonate – role of dual therapy: A case report and review of literature

Journal of Indian Association of Pediatric Surgeons, 2020
Kaposiform hemangioendothelioma (KHE) represents a rare, borderline vascular tumor with locally aggressive behavior. They are often associated with a potentially life-threatening coagulopathy known as Kasabach–Merritt phenomenon (KMP).
Gaurav Parashar, Gowri Shankar, Ravindra Sahadev, Ramesh Santhanakrishnan   +3 more
doaj   +1 more source

Additive value of transarterial embolization to systemic sirolimus treatment in kaposiform hemangioendothelioma. [PDF]

, 2020
Kaposiform hemangioendothelioma (KHE) is a rare vascular tumor in children, which can be accompanied by life-threatening thrombocytopenia, referred to as Kasabach-Merritt phenomenon (KMP).
Richard Brill, Huf, Veronika, Beate Häberle, Jacob Neumann, Moritz Wildgruber, Heid, Esther, Schinner, Regina, Sporns, Peter B., Wohlgemuth, Walter A., Lauten, Melchior, Wibke Uller, Till, Anne‐Marie, Regina Schinner, Brill, Richard, Häberle, Beate, Hüsemann, Dieter, Anne‐Marie Till, Schmidt, Vanessa F, Veronika Huf, Kapp, Friedrich G., Müller-Wille, René, René Müller‐Wille, Uller, Wibke, Dieter Hüsemann, Alexandra Pohl, Jens Ricke, Walter A. Wohlgemuth, Schmid, Axel, Jochen Rössler, Güttel, Christian, Peter B. Sporns, Friedrich G. Kapp, Schmidt, Vanessa F., Irene Schmid, Katrin Funke, Ricke, Jens, Ziermann, Franziska, Lutz Meyer, Meyer, Lutz, Schmid, Irene, Vanessa F. Schmidt, Esther Heid, Kapp, Friedrich G, Perkowski, Sybille, Till, Anne-Marie, Christian Güttel, Melchior Lauten, Sporns, Peter B, Sybille Perkowski, Rössler, Jochen, Wildgruber, Moritz, Pohl, Alexandra, Axel Schmid, Funke, Katrin, Neumann, Jacob, Franziska Ziermann, Müller‐Wille, René, Wohlgemuth, Walter A   +57 more
core   +2 more sources

Musculoskeletal complication in kaposiform hemangioendothelioma without Kasabach–Merritt phenomenon: clinical characteristics and management

, 2018
Yi Ji,1 Kaiying Yang,1 Siyuan Chen,2 Suhua Peng,1 Guoyan Lu,3 Xingtao Liu4 1Division of Oncology, Department of Pediatric Surgery, West China Hospital of Sichuan University, Chengdu, China; 2Pediatric Intensive Care Unit, Department of Critical Care ...
Liu X, Lu G, Yang K, Peng S, Ji Y, Chen S   +5 more
core  

Transcriptomic Profiling Unveils EDN3+ Meningeal Fibroblasts as Key Players in Sturge‐Weber Syndrome Pathogenesis

Advanced Science, Volume 12, Issue 17, May 8, 2025.
Sturge‐Weber syndrome (SWS) is characterized by leptomeningeal vascular malformations, leading to seizures and stroke. Analysis of 119 446 brain cells from SWS patients uncovered distinct cell heterogeneity and identified an EDN3⁺ meningeal fibroblast cluster, with WNT5A emerging as a potential key driver of SWS progression and a promising therapeutic ...
Daosheng Ai, Tianyue Ming, Xiaoli Li, Shu Wang, Zhanying Bi, Jinyi Zuo, Zizhang Cheng, Weijin Sun, Mingguo Xie, Fengzhi Li, Xiongfei Wang, Xueling Qi, Guoming Luan, Woo‐ping Ge, Yuguang Guan   +14 more
wiley   +1 more source

Kaposiform hemangioendothelioma further broadens the phenotype of PIK3CA-related overgrowth spectrum

, 2021
Kaposiform hemangioendothelioma (KHE) is a rare locally aggressive mixed vascular tumor, with typical onset in early childhood and characterized by progressive angio- and lymphangiogenesis. Its etiopathogenesis and molecular bases are still unclear. Here,
Ferrero G. B., Coppo P., Santoro F., Mussa A., Cardaropoli S., Carli D., Ranieri C., Francia di Celle P., Fagioli F., Resta N., La Selva R., Kalantari S., Manicone R.   +12 more
core   +1 more source