Results 61 to 70 of about 14,208 (216)

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

open access: yesPrenatal 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   +11 more
wiley   +1 more source

Pink Polypoid Papulo‐Vesicles on Labia Majora

open access: yes
JEADV Clinical Practice, EarlyView.
Maria Chiara Mercuri   +3 more
wiley   +1 more source

Psychosocial Impact of Sarcoma: Challenges and Adaptation, a Meta‐Synthesis

open access: yesPsycho-Oncology, Volume 35, Issue 7, July 2026.
ABSTRACT Objectives Sarcoma is a rare and heterogeneous cancer frequently associated with significant psychosocial burden. This review aims to synthesise qualitative research to examine the psychosocial impact of sarcoma in adults, focusing on how individuals experience and make sense of disruption across diagnosis, treatment, recovery, and ...
R. Beghean   +5 more
wiley   +1 more source

Epithelioid hemangioendothelioma of the submandibular gland [PDF]

open access: yes, 2008
Epithelioid hemangioendothelioma (EH) is a seldom tumor of vascular origin, which occurs at sites such as liver, lung or soft tissues, and has a highly unpredictable malignant potential and clinical course.
MUTU, Vahit   +5 more
core   +1 more source

Hepatic Epithelioid Hemangioendothelioma [PDF]

open access: yes, 2020
The paper gives a clinical example of diagnosing hepatic epithelioid hemangioendothelioma. With allowance made for that the tumor occurs rarely (less than 1% of cases of all vascular tumors), the authors provide the clinical example to demonstrate the ...
I. S. Skrynnikov   +6 more
core   +2 more sources

Epithelioid hemangioendothelioma of the temporal artery presenting as temporal arteritis: Case report and literature review

open access: yesRare Tumors, 2009
Hemangioendotheliomas are classified as epithelioid hemangioendothelioma(EHE), retiform hemangioendothelioma, composite hemanioendothelioma, Kaposiform hemangioendothelioma (with or without Kasabach-Merritt syndrome), and Spindle cell ...
Salem Alowami   +2 more
doaj   +1 more source

The Top Five Advances in Solid Organ Transplantation in the Past Fifty Years

open access: yes
World Journal of Surgery, EarlyView.
Stephen J. Wigmore, Diana A. Wu
wiley   +1 more source

Ossifying spindled and epithelioid tumour: Expanding the clinical and morphologic spectrum of a recently described entity

open access: yesHistopathology, Volume 89, Issue 1, Page 163-173, July 2026.
Ossifying spindled and epithelioid tumour (OSET) can show unusual morphologic features, including minimal or absent peripheral ossification, eosinophil‐rich stroma, increased mitotic activity (≥5 mitotic figures per 10 high‐power fields), and necrosis.
Rayan M Sibira   +9 more
wiley   +1 more source

Epithelioid hemangioendothelioma in a Child

open access: yesJournal of Cutaneous and Aesthetic Surgery, 2013
Epithelioid hemangioendothelioma (EHE) is a rare tumour arising from the vascular endothelium of soft-tissue, bone and viscera. Skin involvement is rare. The disease has an indolent course, with the potential for recurrence and often associated with multi-systemic localisations.
Madura, C   +3 more
openaire   +2 more sources

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