Results 41 to 50 of about 1,161,166 (152)

[Propranolol treatment in Kasabach-Merritt Syndrome secondary to congenital hepatic hemangioma. Clinical case]

, 2021
Disponible en: https://www.sap.org.ar/docs/publicaciones/archivosarg/2021/v119n1a26.pdfAbstract in English, Spanish Hepatic hemangioma is the most common benign liver tumor.
Selzer, Erika., Malla, Ivone.
core   +1 more source

Outcomes of Live Virus Vaccination in Patients With Vascular Anomalies Being Treated With Sirolimus

Pediatric Blood &Cancer, Volume 73, Issue 7, July 2026.
ABSTRACT Background Live vaccination in patients with vascular anomalies (VA) receiving sirolimus remains controversial due to immunosuppressive effects and theoretical risks. Procedure This single‐center retrospective study included patients with VA less than 4 years old at the start of sirolimus therapy who were incompletely vaccinated.
Svatava Merkle, Kiersten Ricci, Kelly Blache, Rebecca A. Marsh, Adrienne M. Hammill, Elissa Engel   +5 more
wiley   +1 more source

Prenatal Diagnosis and Management of Kaposiform Hemangioendothelioma With Kasabach–Merritt Phenomenon: Imaging Features and First Experience With Maternal Sirolimus Therapy

Prenatal Diagnosis, Volume 46, Issue 8, Page 1278-1285, July 2026.
ABSTRACT Objective To describe the prenatal diagnosis, evolution, and perinatal management of kaposiform hemangioendothelioma (KHE) complicated by the Kasabach–Merritt phenomenon (KMP), and to report the first documented use of maternal sirolimus therapy (MST) in this setting. Methods We retrospectively reviewed four fetuses with a prenatal soft‐tissue
Antoine Fraissenon, Chris Minella, Marion Bordas‐Fournel, Anne Gaëlle Grebille, Olivia Boccara, Marie Cassart, Sarah Simon‐Locatelli, Gwenaelle André, Guillaume Canaud, Alexandre Guilhem, Sara Cabet, Laurent Guibaud   +11 more
wiley   +1 more source

Recurrent multifocal cutaneous Kaposiform hemangioendothelioma: A rare vascular tumor of infancy and childhood

Indian Journal of Pathology and Microbiology, 2016
Kaposiform hemangioendothelioma (KHE) is a locally aggressive vascular tumor of childhood although cases occurring in adulthood are also described. The features overlap with juvenile capillary hemangioma and Kaposi sarcoma.
Bhagyalakshmi Atla, P V Sudhakar, Nagarjun Rao, Uma Prasad   +3 more
doaj   +1 more source

Targeted Therapies in Infantile Hemangiomas and Vascular Malformations: From β‐Blockers to PI3K/AKT/mTOR Inhibitors

Journal of Cellular and Molecular Medicine, Volume 30, Issue 7, April 2026.
ABSTRACT Vascular tumours and malformations encompass infantile hemangiomas (IHs) and genetically driven vascular malformations with distinct natural histories and therapeutic vulnerabilities. The discovery that the non‐selective beta‐blocker propranolol induces rapid regression of proliferating IHs established the first widely adopted systemic ...
Hubert Arasiewicz, Michal Dec
wiley   +1 more source

Giant hepatic hemangioma with Kasabach-Merritt syndrome treated with right hepatectomy: a case report with literature review

, 2023
Background: We present a case of giant hepatic hemangioma with Kasabach-Merritt syndrome. Material and methods: A thirty-seven-year-old female presented to us with a six-month history of recurrent abdominal pain and weight loss.
Vasavada, Bhavin, Patel, Hardik
core   +1 more source

CLINICAL CASE: THE SYNDROME OF KASABACH-MERRITT (SCM)

Актуальные проблемы теоретической и клинической медицины, 2022
Relevance. Kazabach-Merritt syndrome is extremely rare in children's practice. Clinical manifestations are diverse, which complicates the timely diagnosis and treatment of this di sease.Purpose: to attract the attention of pediatricians, neonatologists ...
G. N. Balmagambetova, S. A. Lisogor, V. M. Shmonin   +2 more
doaj   +1 more source

Primary hepatic angiosarcoma: A case-based discussion of unique presentations and extrahepatic manifestations

Current Problems in Cancer: Case Reports, 2020
Hepatic angiosarcoma is a rare and heterogeneous neoplasm that carries with it an especially poor prognosis. Diagnosis is challenging given that patients often present with vague, nonspecific complaints, and early multiorgan dysfunction has the potential
Brandon K.K. Fields, George R. Matcuk, Jr, Doan Lai, Andrew Lee, Sami Dwabe, Courtney Hanlon, Natalie L. Demirjian, Seth Politano   +7 more
doaj   +1 more source

A Rare Case of Neonatal Kaposiform Hemangioendothelioma With Kasabach–Merritt Phenomenon Presenting as an Abdominal Mass Without Cutaneous Manifestations

Case Reports in Hematology, Volume 2026, Issue 1, 2026.
Kaposiform hemangioendothelioma (KHE) is a rare vascular neoplasm that typically presents in infancy or early childhood, classified as a locally aggressive/borderline vascular tumor. It most commonly involves superficial and deep soft tissues, often demonstrating infiltrative growth into adjacent muscle and bone, whereas retroperitoneal or ...
Su Young Park, Amrryn Halari, Jessenia Palacio-Meadows, Nehal S. Parikh, Danielle Bentsen, Surasak Puvabanditsin, Kalyani Sen   +6 more
wiley   +1 more source

Radiotherapy in Kasabach-Merritt syndrome

, 1997
A male infant was born with a 1 x 3 cm reddish lesion under his umbilicus which enlarged within a month and was associated with consumptive coagulopathy. A diagnosis of Kasabach-Merritt syndrome (KMS) was made.
Arif Bülent Aras, Özsaran Z., Deniz Yalman, Ayfer Haydaroǧlu, Yalman D., Haydaroglu A., Zeynep Özsaran, Aras A.B., Esassolak M., Nazan Çetingül, Çetingül N., Mustafa Esassolak   +11 more
core   +1 more source