Results 41 to 50 of about 4,977 (176)

Management of Kaposiform Haemangioendothelioma—A Retrospective Case Series Examining the Use and Effectiveness of Vincristine

Journal of Paediatrics and Child Health, EarlyView.
ABSTRACT Aim Kaposiform haemangioendothelioma is a rare vascular tumour. Management has evolved over the last two decades, with most cases receiving vincristine or sirolimus. We aim to describe our experience with managing this tumour, with a focus on the safety and efficacy of vincristine.
Bronwen Kirk, Susan Adams, Orli Wargon, Artiene Tatian, Susan Russell   +4 more
wiley   +1 more source

Nail Clubbing‐Associated With a Large Segmental Infantile Hemangioma of the Arm in a Patient With PHACES Syndrome

Pediatric Dermatology, EarlyView.
ABSTRACT Although infantile hemangiomas (IH) are common vascular tumors of childhood, associated nail abnormalities are rare. We report a child with a large segmental IH of the upper limb with marked, ipsilateral nail clubbing, which gradually improved until the age of 7 years.
Stefan Blunder, Lisa Weibel, Nicole Knöpfel, Martin Theiler, Agnes Schwieger‐Briel, Isabelle Luchsinger   +5 more
wiley   +1 more source

Successful propranolol therapy for infantile hepatic hemangioma with cardiac failure

JPGN Reports, Volume 7, Issue 3, Page 387-390, August 2026.
Abstract Infantile hepatic hemangioma (IHH) can cause severe complications such as high‐output cardiac failure and growth faltering, requiring prompt diagnosis and intervention. In the absence of standardized treatment guidelines, propranolol has emerged as an effective and well‐tolerated therapy.
Fadhel Al Ateeqi, Ala K. Shaikhkhalil, Haitham Talo, Naeem Jagirdar, Mahdia AL‐Haidar   +4 more
wiley   +1 more source

Biology of Infantile Hemangioma [PDF]

Frontiers in Surgery, 2014
Infantile hemangioma (IH), the most common tumor of infancy, is characterized by an initial proliferation during infancy followed by spontaneous involution over the next 5-10 years, often leaving a fibro-fatty residuum. IH is traditionally considered a tumor of the microvasculature.
Tinte eItinteang, Aaron HJ Withers, Aaron HJ Withers, Paul F Davis, Swee Thong Tan   +4 more
openaire   +3 more sources

Bayesian Estimation of the Binomial Parameter in Adaptive Designs With Treatment Selection

Statistics in Medicine, Volume 45, Issue 18-19, August 2026.
ABSTRACT It is well‐known that results from adaptive multi‐arm experiments with treatment selection are subject to the bias of the selection process. In this article, we consider designs with a binary outcome that begin with randomized parallel arms.
Pierre Bunouf, Jean‐Marie Boher
wiley   +1 more source

Two Cases of Oculofaciocardiodental (OFCD) Syndrome due to X-Linked BCOR Mutations Presenting with Infantile Hemangiomas: Phenotypic Overlap with PHACE Syndrome

Case Reports in Genetics, 2019
Background. Oculofaciocardiodental (OFCD) syndrome is due to mutations in BCOR (BCL-6 corepressor). OFCD has phenotypic overlaps with PHACE syndrome (Posterior fossa anomalies, Hemangioma, Arterial anomalies, Cardiac defects, Eye anomalies).
T. M. Morgan, J. M. Colazo, L. Duncan, R. Hamid, K. M. Joos   +4 more
doaj   +1 more source

Sclerotherapy for the treatment of infantile hemangiomas

Journal of Cutaneous and Aesthetic Surgery, 2012
Sclerotherapy is a simple, technically easy and effective mode of treatment for infantile hemangiomas (IH). It acts by blocking the growth of actively proliferating lesions, by targeting their vascularity accelerating their regression. Polidocanol is a commonly used sclerosant.
Grover, Chander, Khurana, Ananta, Bhattacharya, Sambit N   +2 more
openaire   +2 more sources

Maternal propranolol as a safe alternative to invasive fetal surgery in chorioangioma management

Ultrasound in Obstetrics &Gynecology, Volume 68, Issue 2, Page 284-288, August 2026.
ABSTRACT Chorioangiomas are associated with a significant risk of fetal demise due to high‐output cardiac failure. Standard invasive treatment, including fetoscopic laser photocoagulation and intratumoral embolization, shows limited success and has high fetal mortality rates.
L. E. van der Meeren, F. Slaghekke, S. Zaaijer, F. Prein, E. Lopriore, M. C. Haak   +5 more
wiley   +1 more source

Treatment of large cutaneous facial hemangioma with propranolol in a child with biliary atresia and esophageal varices

Caspian Journal of Pediatrics, 2017
Introduction:  Biliary atresia (BA) is the most common cause of neonatal jaundice, for which surgery is indicated. It may lead to portal hypertension and esophageal varices. Sometimes, BA is related to other congenital anomalies and malformation, while a
Mohammad Reza Esmaeili Dooki, Abbas Hadipour, Sanaz Mehrabani, Neda Joghtaei, Hajighorban Noreddini, Mehrangiz Amiri, Mohammadreza Salehiomran   +6 more
doaj  

A Case of Slow Progressive Cutaneous Angiomatosis on a Cat Metatarsal Pad Treated by a Topical Beta‐Blocker

Veterinary Dermatology, Volume 37, Issue 4, Page 530-533, August 2026.
ABSTRACT A 5‐year‐old female cat presented with a purple depressed lesion on a metatarsal pad inducing ulceration and pain. Histopathological results revealed a non‐neoplastic vascular proliferation, a rare condition in cats. Topical beta‐blocker successfully prevented recurrence of ulceration.
Adrien Accard, Rita Bitar, Maria Dolores Sanchez, Philippe Blumstein, Olivier Albaric, Nora Bouhsina, Emmanuel Bensignor   +6 more
wiley   +1 more source