[Intravascular papillary endothelial hyperplasia (IPEH) : Masson's pseudoangiosarcoma on the forefoot].

Orthopade

Orthopädie und orthopädische Rheumatologie, Elisabeth-Klinik Bigge, Heinrich-Sommer-Straße 4, 59939, Olsberg, Deutschland.

Published: April 2017

Intravascular papillary endothelial hyperplasia (IPEH)/Masson's pseudoangiosarcoma is a rare (orphan) disease of the forefoot that has not yet been described in Europe. The pathoanatomic examination of a young patient with a vague interdigital space-consuming lesion revealed a intravascular papillary endothelial hyperplasia/Masson's pseudoangiosarcoma. The intravascular papillary endothelial hyperplasia can be mainly detected in the upper limbs as well as cervically. Heretofore, the intravascular papillary endothelial hyperplasia has only been described in Japan and the USA. For Europe, our case report is the first description of the clinical course of IPEH.

Download full-text PDF

Source
http://dx.doi.org/10.1007/s00132-017-3396-4DOI Listing

Publication Analysis

Top Keywords

papillary endothelial
20
endothelial hyperplasia
16
intravascular papillary
12
endothelial
5
[intravascular papillary
4
hyperplasia
4
hyperplasia ipeh
4
ipeh masson's
4
masson's pseudoangiosarcoma
4
pseudoangiosarcoma forefoot]
4

Similar Publications

Intravascular Papillary Endothelial hyperplasia (IPEH) are benign vascular lesions rarely described in the pediatric population. We present here the case and the management of a 11-year-old child with a lateral neck mass. The diagnosis of IPEH can be challenging for the clinician and the radiologist as it may mimic other pathologic entities.

View Article and Find Full Text PDF

Background: Generalized lymphatic anomaly (GLA) is a rare congenital lymphatic malformation (LM) characterized by multiple infiltrating lymphangiomas in various tissues. Owing to its rarity, information on this disease is obtained mainly through case reports, leading to delayed diagnosis. In this study, we reported a case of generalized lymphatic anomaly in a pediatric patient manifesting as hemorrhagic pleural effusion.

View Article and Find Full Text PDF

Background: Muscle-invasive bladder cancer (MIBC) is a prevalent cancer characterized by molecular and clinical heterogeneity. Assessing the spatial heterogeneity of the MIBC microenvironment is crucial to understand its clinical significance.

Methods: In this study, we used imaging mass cytometry (IMC) to assess the spatial heterogeneity of MIBC microenvironment across 185 regions of interest in 40 tissue samples.

View Article and Find Full Text PDF

Non-clear cell renal cell carcinoma narrative review: where we are in 2024.

Transl Cancer Res

November 2024

Division of Hematology and Oncology, Department of Internal Medicine, Froedtert & the Medical College of Wisconsin, Milwaukee, WI, USA.

Article Synopsis
  • Advances in understanding non-clear cell renal cell carcinoma (RCC) have improved due to better molecular and genetic testing, helping to identify specific subtypes and personalize treatment.
  • Representation in clinical trials for rare non-papillary RCC variants is limited, making evidence-based management difficult.
  • The shift toward molecular diagnostics is enhancing our knowledge of RCC behaviors and responses to treatments, although most evidence comes from smaller clinical studies rather than extensive trials.
View Article and Find Full Text PDF
Article Synopsis
  • Optic disc melanocytoma is a benign, usually asymptomatic tumor found in the eye, but it can lead to complications like choroidal neovascularization, which can be challenging to distinguish from malignant tumors.
  • A case study of a 54-year-old man with optic disc melanocytoma showed the need for close monitoring due to growth, prompting treatment with anti-VEGF-A injections after development of neovascular membranes.
  • Treatment with intravitreal anti-VEGF-A can effectively manage choroidal neovascularization related to optic disc melanocytoma and requires advanced imaging techniques for accurate diagnosis.
View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!