Results 61 to 70 of about 1,161,166 (155)

Kasabach-merritt syndrome arising from tufted angioma successfully treated with systemic corticosteroid [PDF]

open access: yes, 2010
We report a case of Kasabach-Merritt syndrome arising from a tufted angioma successfully treated with systemic corticosteroid. A 2-month-old male infant presented with a palm-sized, erythematous induration on his left pubis.
Kee Yang Chung   +5 more
core   +1 more source

Bleomycin‐Elektrosklerotherapie bei kaposiformem Hämangioendotheliom mit Kasabach‐Merritt‐Phänomen im Erwachsenenalter

open access: yes
JDDG: Journal der Deutschen Dermatologischen Gesellschaft, Volume 24, Issue 4, Page 551-553, April 2026.
Jakob Veeser   +11 more
wiley   +1 more source

Advancing Precision Medicine: The Role of Genetic Testing and Sequencing Technologies in Identifying Biological Markers for Rare Cancers

open access: yesCancer Medicine, Volume 14, Issue 8, April 2025.
ABSTRACT Background Genetic testing and sequencing technologies offer a comprehensive understanding of cancer genetics, providing rapid and cost‐effective solutions. In particular, these advanced technologies play an important role in assessing the complexities of the rare cancer types affecting several systems including the bone, endocrine, digestive,
Joviana Farhat   +4 more
wiley   +1 more source

Ultrasound‐Guided Percutaneous Sclerotherapy With Bleomycin for Management of Infantile Subcutaneous Hemangioma: A Case Report

open access: yesClinical Case Reports, Volume 13, Issue 2, February 2025.
ABSTRACT Percutaneous sclerotherapy with bleomycin is an effective, minimally invasive treatment for aggressive pediatric hemangiomas, especially when traditional therapies fail. This approach can improve clinical outcomes, including thrombocytopenia resolution and tumor size reduction, with minimal systemic side effects.
Iman Kiani   +4 more
wiley   +1 more source

Kasabach-Merritt syndrome: clinical vs. surgical treatment

open access: yesJornal Vascular Brasileiro, 2014
Kassabach-Merritt syndrome is a combination of capillary hemangioma and thrombocytopenia that predisposes to bleeding with petechiae, ecchymosis and spontaneous bruising.
Regina Moura   +7 more
doaj   +1 more source

Sirolimus treatment for intractable vascular anomalies (SIVA): An open‐label, single‐arm, multicenter, prospective trial

open access: yesPediatrics International, Volume 67, Issue 1, January/December 2025.
Abstract Background Intractable vascular anomalies (VAs), including vascular tumors and venous, lymphatic, and mixed malformations, often have severe symptoms and a poor prognosis, highlighting the need for new treatments. We conducted a prospective trial of sirolimus (tablet and granule forms) for the treatment of VAs.
Michio Ozeki   +23 more
wiley   +1 more source

Ovarian hemangioma: A rare encounter

open access: yesClinical Case Reports, Volume 12, Issue 9, September 2024.
Key Clinical Message Ovarian hemangioma, though rare and asymptomatic, can mimic malignant ovarian tumors, thus it is necessary for comprehensive histopathological and immunohistochemical evaluation for accurate diagnosis and appropriate management.
M. Singh   +6 more
wiley   +1 more source

Cardiac interventricular septum hemangioma in a colon cancer patient treated with Capecitabine: A case report and review of literature

open access: yesClinical Case Reports, Volume 12, Issue 8, August 2024.
Young male with stage IIIB sigmoid colon adenocarcinoma, treated with XELOX (Oxaliplatin + Capecitabine), developed atypical chest pain, shortness of breath, and tachycardia after Capecitabine. Various cardiac imaging led to hemangioma diagnosis. Capecitabine's arterial vasospasm induction may explain the transient ischemic presentation.
Yasamin Afsari Zonooz   +7 more
wiley   +1 more source

A Case Report of Scapular Hemangioma with Kasabach–Merritt Syndrome: An Insight into Various Treatment Strategies with Review of Literature

open access: yesIndian Journal of Medical and Paediatric Oncology
Hemangiomas are common tumors, accounting for 4 to 5% of all benign tumors in infancy and childhood. While they typically occur superficially, their presence in bone is extremely rare.
Rajesh Bahadur Singh   +5 more
doaj   +1 more source

Kasabach-Merritt syndrome with large cutaneous vascular tumors

open access: yesJournal of Indian Association of Pediatric Surgeons, 2012
A case series of four patients who presented with large surface vascular tumors and low platelet count and their management is reported. Medical management was done with steroids, propranolol and vincristine in different combinations.
Pavai Arunachalam   +2 more
doaj   +1 more source

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