A case of benign vascular tumor of the ankle is presented, along with a history and classification of hemangiomas and hemangiopericytomas. The primary diagnosis was hypertrophic hemangioma or hemangiopericytoma. Differentiating these tumors was difficult because staining techniques did not readily separate endothelial from pericytic cells. This is a discussion of two vascular tumors, both of which are uncommon in the foot, and their similarities and differences are contrasted. Clinical and pathologic presentations, operative treatments, and further differential diagnosis are also discussed.
Download full-text PDF |
Source |
|---|
Publication Analysis
Top Keywords
Similar Publications
Klippel-Trenaunay Syndrome: A Case Study of Severe Anemia in a Rare Vascular Disorder.
Cureus
December 2024
Internal Medicine Department, Hamad Medical Corporation, Doha, QAT.
Klippel-Trenaunay syndrome (KTS) is a rare congenital vascular disorder involving varicosities, cutaneous vascular malformations, and hypertrophy of soft tissues and bones. It is often linked to gene mutations. It affects the lymphatic, capillary, and venous systems.
View Article and Find Full Text PDFActeoside relieves diabetic retinopathy through the inhibition of Müller cell reactive hyperplasia by regulating TXNIP and mediating Kir4.1 channels in a PI3K/Akt-dependent manner.
PLoS One
December 2024
Ophthalmology Department, The First Affiliated Hospital of Kunming Medical University, Kunming, China.
Diabetic retinopathy (DR) is a severe microangiopathy of diabetes. Müller cells play an important role in the development of DR. Acteoside (ACT) has been reported to be effective in the treatment of DR.
View Article and Find Full Text PDFLittoral cell angioma of the spleen in a 70-year-old male patient with myelodysplastic syndrome: a case report.
Cir Cir
November 2024
Department of Surgery, School of Medicine, Aristotle University of Thessaloniki.
Introduction: Littoral cell angioma (LCA) is a new subtype of vascular tumor, which has been reported infrequently worldwide. It is associated with visceral malignancies and other immunologic conditions.
Clinical Case: We present a case of a 70-year-old Caucasian male with a 6-year history of myelodysplastic syndrome, which was investigated for splenomegaly and pancytopenia.
Unusual co-occurrence of hypertrophic inferior olivary degeneration with infratentorial cavernomatosis and orbital cavernous hemangioma.
Radiol Case Rep
January 2025
Radiology Department, Mohammed Vth military hospital, 10010 Rabat, Morocco.
Article Synopsis
- * Cavernomas and orbital cavernous hemangiomas are specific types of vascular malformations linked to HOD, but their combination is extremely rare, with only one previous case reported.
- * A notable case involved a 26-year-old male with eye bulging and myoclonus, where MRI revealed HOD from cavernous malformations, highlighting the need to consider vascular issues as potential causes of HOD.
Sporadic hypertrophic and nodular port-wine stain: a study of 27 cases with emphasis on histological features and novel mutation type.
J Clin Pathol
October 2024
Department of Pathology, Henan Provincial People's Hospital, the People's Hospital of Zhengzhou University, Zhengzhou, Henan, China
Aims: To investigate the clinicopathological features and molecular characteristics of sporadic hypertrophic and nodular port-wine stains (PWS).
Methods: We analysed the clinicopathological and molecular characteristics of 27 sporadic hypertrophic and nodular PWS retrieved from our pathology database from 2013 to 2023 and reviewed the relevant literature.
Results: There were 13 men and 14 women who ranged in age from 10 to 66 years.
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!