Results 61 to 70 of about 4,369 (185)

Lymphangiomatosis – A Rare Disease in Pediatrics

open access: yes, 2015
Lymphangiomatosis is rare in both adults and children. We present an 11 year old boy with right chylothorax. The formation of chylothorax was a result of diffuse lymphangioma in the mediastinum spreading to the pleura.
Tuan DM   +5 more
core   +1 more source

Generalized cystic lymphangiomatosis [PDF]

open access: yesPediatric Radiology, 2010
A 2-year-old girl presented with acute shortness of breath and multiple subcutaneous nodules. Chest radiograph showed widening of the mediastinum. Contrast-enhanced CT of the thorax revealed interstitial thickening, lung nodules, pleural effusions (Fig. 1a, black arrow) and cystic mediastinal collections (Fig. 1a, white arrow).
Darshana D, Rasalkar, Winnie C W, Chu
openaire   +2 more sources

US, CT and MRI findings in a case of diffuse lymphangiomatosis and cystic hygroma

open access: yes, 2008
Lymphangiomatosis is a rare disease with multifocal lymphatic proliferation that typically occurs during childhood and involves multiple parenchymal organs including the lung, liver, spleen, bone, and skin.
Erturk, S. M.   +5 more
core   +1 more source

Trametinib normalizes angiopoietin-2 levels and successfully treats kaposiform lymphangiomatosis. [PDF]

open access: yesJ Vasc Anom (Phila)
Kaposiform lymphangiomatosis (KLA) is a complex lymphatic anomaly with high morbidity and mortality. Angiopoietin-2 (Ang-2) levels are elevated in the blood of patients with KLA and can be used to aid in diagnosis and monitor treatment response.
McDaniel CG   +6 more
europepmc   +2 more sources

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

open access: yesJournal 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

Lymphangiomatosis

open access: yes, 2013
Clinical History Image Findings Discussion Find Diagnosis Differential ...
openaire   +2 more sources

Surgical Treatment for Benign Lymphangioendothelioma After Two Incomplete Excisions: A Case Report and Literature Review

open access: yesClinical, Cosmetic and Investigational Dermatology, 2023
Wei Lu,1 Yan Cao,2 Fanhua Zeng,1,3 Chun Chen,1,4 Zhenyu Yang,1 Zuoliang Qi,1 Xiaonan Yang1 1The Department of Hemangioma and Vascular Malformation, Plastic Surgery Hospital, Chinese Academy of Medical Sciences (CAMS) and Peking Union Medical College ...
Lu W   +6 more
doaj  

Imaging Features of Lymphatic Malformation in Children

open access: yesCT Lilun yu yingyong yanjiu, 2022
Lymphangiodysplasia is a common vascular disease in children. This paper summarizes the imaging characteristics, anatomical basis and pathophysiological mechanism of lymphatic reflux disorder, lymphangiodilation, lymphangiopathy and lymphangiomatosis ...
Qifeng ZHANG   +4 more
doaj   +1 more source

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

open access: yesCase 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   +6 more
wiley   +1 more source

Diffuse pulmonary lymphangiomatosis

open access: yesHuman Pathology, 1993
Angiomatous lesions of the lung are uncommon and not well characterized. We describe nine cases of a distinct lymphatic vascular lesion that we have termed "diffuse pulmonary lymphangiomatosis." Extrathoracic lymphangiomatous lesions were not identified. The patients comprised seven males and two females with a mean age at presentation of 10 years (age
H D, Tazelaar   +5 more
openaire   +2 more sources

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