Peliosis of the spleen.

Gastrointest Radiol

Department of Radiology, Groote Schuur Hospital/University of Cape Town, South Africa.

Published: March 1991

The authors present a case of splenic peliosis in a 32-year-old woman who had been treated with steroids for asthma. The ultrasound, computed tomographic (CT), and angiographic findings of this entity are herein illustrated.

Download full-text PDF

Source
http://dx.doi.org/10.1007/BF01887312DOI Listing

Publication Analysis

Top Keywords

peliosis spleen
4
spleen authors
4
authors case
4
case splenic
4
splenic peliosis
4
peliosis 32-year-old
4
32-year-old woman
4
woman treated
4
treated steroids
4
steroids asthma
4

Similar Publications

Immune thrombocytopenia (ITP) is a common hematological disorder. Our previous study has found that exosomal miR-146a-5p derived from bone marrow mesenchymal stromal cells (BMSCs) regulate Th17/Treg balance to alleviate ITP. This work further investigated the role of miR-146a-5p in ITP with pregnancy.

View Article and Find Full Text PDF

Background: Cytotoxic T lymphocyte-associated antigen-4 (CTLA-4) insufficiency is a rare disease belonging to inborn errors of immunity. Most cases of patients with CTLA-4 insufficiency are diagnosed in adults, therefore it is not a common problem in the clinical practice of pediatricians. However, it is worth noticing that most cases described in the literature show the first symptoms of the disease before the age of 18, but the phenotypic variability of patients complicates and delays the diagnostic process.

View Article and Find Full Text PDF
Article Synopsis
  • Fostamatinib is an approved treatment for adults with chronic immune thrombocytopenia (ITP) but there's limited research on tapering doses and achieving remission after stopping the drug.
  • A study involving 61 patients examined the safety and effectiveness of fostamatinib during and after dose tapering, noting that complete platelet response was typically achieved within 28 days.
  • Results showed that most patients maintained platelet counts above 100 × 10/L after discontinuation, with a low relapse rate, suggesting that tapering could lead to sustained remission, though further research on tapering strategies is needed.
View Article and Find Full Text PDF

Background: The characteristic feature of immune cytopenias involves the process of extravascular phagocytosis, wherein macrophages in the spleen and/or liver engage in the destruction of blood cells that have been opsonized by auto- or alloantibodies. Therefore, new treatments that prevent phagocytosis will be advantageous, especially for short-term usage along with alternative options.

Study Design And Methods: KB-208, a small molecule drug, previously shown to be efficacious for the in vitro inhibition of phagocytosis was synthesized.

View Article and Find Full Text PDF

Rare Case of Idiopathic Thrombocytopenia Causing Retrobulbar Hemorrhage.

J Community Hosp Intern Med Perspect

September 2024

Department of Internal Medicine, CAMC, Charleston, WV, 25304, USA.

Immune thrombocytopenia purpura (ITP) is defined as a platelet count lower than 100 × 10ˆ9/L, in the absence of known abnormalities in white blood cells, normal hemoglobin with generalized purpuric rash: making it a diagnosis of exclusion.1-2 ITP is due to destruction of platelets in the spleen via autoantibodies, resulting in reduced platelet counts.3 Though rare, ITP is linked with spontaneous retrobulbar hemorrhage (SRH).

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!