Results 31 to 40 of about 46,567 (266)

Intranodal capillary-cavernous hemangioma: Report of a very rare case [PDF]

, 2019
Mixed type capillary-cavernous hemangioma is a rare vascular anomaly, with an intranodal localization being extremely rare. Its finding is often accidental but may be clinically symptomatic. The diagnosis relies on histopathology, showing a proliferation
Tessieras, Jérôme, Chenaye, Jinane, Senechaud, Christophe, Christophe Senechaud, Jérôme Tessieras, Banz, Yara, Jinane Chenaye, Yara Banz   +7 more
core   +1 more source

Conventional Hemangioma and Lymphangioma [PDF]

, 2020
Hemangioma of the bone is a benign neoplasm of endothelial cells that form blood vessels. It is one of the most common tumors of bone and has been found in vertebral bodies in approximately 10% of the adult population.
Rosenberg, Andrew E, Yaxia Zhang, Andrew E. Rosenberg, Zhang, Yaxia   +3 more
core   +1 more source

Clinical characteristics of infantile haemangioma in twins: a retrospective study

BMC Pediatrics
Background Infantile hemangioma is one of the most common benign soft tissue tumors in infants. The pathogenesis of infantile hemangioma remains unclear and twin studies regarding its incidence may help clarify disease pathogenesis.
Zhengwei Sun, Miaomiao Li, Changxian Dong, Shiwei Mei   +3 more
doaj   +1 more source

POEMS Syndrome: 2026 Update on Diagnosis, Risk‐Stratification, and Management

American Journal of Hematology, EarlyView.
ABSTRACT Disease Overview POEMS syndrome is a life‐threatening syndrome due to an underlying plasma cell neoplasm. The major criteria for the syndrome are polyneuropathy, clonal plasma cell disorder (PCD), sclerotic bone lesions, elevated vascular endothelial growth factor, and the presence of Castleman disease.
Angela Dispenzieri
wiley   +1 more source

Cardiac hemangioma of the right atrium in a neonate : fetal management and expedited surgical resection [PDF]

, 2005
Cardiac hemangioma is a rare tumor with a reported incidence of 1-2%. We describe the case of a neonate with a right atrial mass that was diagnosed prenatally. The fetus developed a supraventricular tachycardia and was delivered by cesarean section in
Campbell, A., Einzig, Stanley, Kula, Monika, Costello, C., D’Cruz, C.A., Sebastian, Vinod A.   +5 more
core  

The Use of Water-assisted Liposuction for Breast Deformity Induced by Polyacrylamide Hydrogel

Plastic and Reconstructive Surgery, Global Open
Background:. Approximately 200,000 women in China have undergone breast augmentation using polyacrylamide hydrogel (PAAG) injections. However, PAAG injections have been associated with complications such as mastalgia, gel migration, inflammation ...
Yingjie Zhu, MS, Yang Xiong, BS, Mariya M.J. Elakkawi, PhD, Xiangdong Qi, MD, PhD   +3 more
doaj   +1 more source

Assessment of Growth in Cardio‐Facio‐Cutaneous Syndrome

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Cardio‐facio‐cutaneous (CFC) syndrome is a rare, multiple congenital anomaly disorder in which individuals commonly experience faltering growth; however, systematic analysis of growth parameters in this disorder has not been performed. We recruited 69 participants with CFC through CFC International and collected data on assessing height ...
Kari Johnston, Sandesh C. S. Nagamani, Bradley S. Miller, Katherine A. Rauen, Richard D. Boyce, Salma Musaad, Pilar L. Magoulas   +6 more
wiley   +1 more source

Capillary hemangioma of tympanic cleft [PDF]

, 2009
We present an extensive capillary hemangioma of right ear in an 11-year-old child involving external auditory canal, middle ear and mastoid. Patient was presented with chronic purulent discharge and aural mass in right ear. The Computarize tomography (CT)
Tiwary, Awadhesh, Rakesh Kumar Singh, Sangita Bhandary, Smirti Karki, Bhandary, Sangita, Singh, Rakesh Kumar, Karki, Smirti, Awadhesh Tiwary   +7 more
core  

Decoding Parkinson's Disease: The interplay of cell death pathways, oxidative stress, and therapeutic innovations

Redox Biology
Parkinson's disease (PD), a complex neurodegenerative disorder characterized by selective loss of substantia nigra (SN) dopaminergic neurons, pathological aggregation of α-synuclein (α-syn), and chronic neuroinflammation, is fundamentally driven by redox
Tingting Liu, Xiangrui Kong, Junbo Qiao, Jianshe Wei   +3 more
doaj   +1 more source

A Novel Splice Variant in ERGIC1 Causes Arthrogryposis Multiplex Congenita—Characterization Using Urine‐Derived Cells

American Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.
ABSTRACT Arthrogryposis multiplex congenita (AMC) is defined as the presence of joint contractures affecting at least two body regions at birth. Three different ERGIC1 variants have been reported in individuals with AMC. Here, we report on a 16‐year‐old male with a homozygous ERGIC1 c.250+1G>A variant that was classified as a variant of uncertain ...
Lauren Kerr, Paul McKay, Juliana Marulanda, Zenghui Wu, Reggie Hamdy, Sena Tavukcu, Noémi Dahan‐Oliel, Frank Rauch   +7 more
wiley   +1 more source