Results 61 to 70 of about 7,852 (206)

A rare cause of abdominal pain: massive splenomegaly and hypersplenism due to Niemann-Pick type-B [PDF]

, 2012
Niemann-Pick disease is a recessive, autosomal hereditary lysosomal storage disease. Six types of the disease have been identified (NPD types A, B, C, D, E, and F).
Arikanoglu, Zulfu, Enver Ay, Firat, Ugur, Ay, Enver, Gul, Mesut, Zulfu Arikanoglu, Ibrahim Aliosmanoglu, Aliosmanoglu, Ibrahim, Mesut Gul, Taskesen, Fatih, Fatih Taskesen   +10 more
core   +1 more source

Wandering Spleen Torsion as A Rare Cause of Acute Abdomen: A Case Report

Clinical Case Reports, Volume 14, Issue 6, June 2026.
ABSTRACT Wandering spleen is a rare clinical condition characterized by excessive mobility of the spleen due to the absence or dysfunction of the ligaments that usually fix the spleen in its natural position. This increased mobility can make the spleen prone to torsion and a variety of complications.
Nader Misagh, Mohammadreza Alipour, Farham Khaksari, Farzane Darrodi, Mohammad Darrodi   +4 more
wiley   +1 more source

Plug-assisted Retrograde Transvenous Obliteration with or without Partial Splenic Embolisation for Gastric Variceal Bleeding: A Retrospective Study [PDF]

Journal of Clinical and Diagnostic Research
Introduction: Gastric variceal bleeding is a severe complication of portal hypertension with limited efficacy of endoscopic therapy in patients with large fundal varices or spontaneous shunts.
Vishal Nandkishor Bakare, Aniketh Davangere Hiremath, Amol Sonyabapu Dahale   +2 more
doaj   +1 more source

Functional Hypersplenism in Mice Induced by Adoptive Transfer of Syngeneic Spleen Cells [PDF]

, 2006
Investigation of peripheral blood cell count alterations in cases with hypersplenism, and an understanding of the relationship between splenic function and hematopoietic cell production require suitable experimental animal models.
Hanna Bessler, Meir Djaldetti, Michael Bergman, Hertzel Salman, Eitan Fibach   +4 more
core   +1 more source

Hypersplenism in a young girl: managed non-surgically [PDF]

, 2017
A 16-years-old female, non-alcoholic, presented with pain in left hypochondrium and distention of abdomen. Her USG Abdomen, portal vein doppler and CT abdomen revealed chronic thrombosis of intrahepatic portion of portal vein with multiple collaterals ...
Gokhale, Vijayashree S., Kakrani, Arjun Lal, Tanvi Batra, Arjun Lal Kakrani, Vijayashree S. Gokhale, Gulati, Shipra, Batra, Tanvi, Shipra Gulati   +7 more
core   +2 more sources

Extrahepatic portal venous obstruction: The effects of early ligation of splenic artery during splenectomy

Journal of Indian Association of Pediatric Surgeons, 2009
Aim: To objectively demonstrate the gain in blood volume and blood components following early ligation of splenic artery during splenectomy and splenorenal shunts in children with extra hepatic portal venous obstruction (EHPVO).
Gazula Suhasini, Pawar D, Seth T, Bal C, Bhatnagar V   +4 more
doaj  

Prognostic Value of the C‐Reactive Protein × Platelet‐to‐Lymphocyte Ratio for 28‐Day Mortality in Patients With Sepsis: A Retrospective Cohort Study

Health Science Reports, Volume 9, Issue 6, June 2026.
ABSTRACT Background and Aims Inflammatory and hematologic biomarkers are commonly used for early risk assessment in sepsis. The C‐reactive protein × platelet‐to‐lymphocyte ratio (CPL) integrates systemic inflammation, platelet‐related thromboinflammation, and lymphocyte‐associated immune suppression. This study aimed to evaluate the association between
Yuping Duan, Yuxuan Zhang, Jiujia Xiao, Mengjiao Yang, Yi Wen, Dan Huang   +5 more
wiley   +1 more source

SUCCESSFUL CHEMOTHERAPY ADMINISTRATION DESPITE HYPERSPLENISM AND PANCYTOPENIA: A CASE OF METASTATIC RECTAL ADENOCARCINOMA

Hematology, Transfusion and Cell Therapy
Introduction: Cytopenias in oncology patients present a significant barrier to the administration of chemotherapy. Hypersplenism is one of the leading causes of cytopenia.
Adil Uğur Kaan Güngör, Abdurrahman Aykut, Berksoy Sahin, Hatice Asoğlu Rüzgar   +3 more
doaj   +1 more source

Development of a Clinical Severity Score for Indian Sickle Cell Anaemia Patients

eJHaem, Volume 7, Issue 3, June 2026.
ABSTRACT Background Sickle cell anaemia (SCA) is a monogenic disorder but shows variable disease severity. We evaluated the utility of paediatric severity scores (PSS) in Indian patients and developed two modified scores: Indian Severity Score 1 (ISS1) by adding four clinical parameters to PSS, and ISS2 by excluding four biochemical measures from ISS1.
Suraj S. Nongmaithem, Amitabh Biswas, Swaroop Iyer, Jandhayala Vyshnavi, Archana Wath, Giriraj R. Chandak, Dipty Jain   +6 more
wiley   +1 more source

Hepatic Monoclonal Light‐ and Heavy‐Chain Deposition Disease Presenting as Noncirrhotic Portal Hypertension With Ascites

Liver International Communications, Volume 7, Issue 2, June 2026.
ABSTRACT Monoclonal immunoglobulin deposition disease (MIDD) is a plasma cell disorder where immunoglobulin light‐ and/or heavy‐chains accumulate in various organs. Hepatic involvement can be challenging to diagnose, as manifestations are protean and Congo red staining is negative.
Bella L. Liu, Helmut G. Rennke, Lei Zhao, Kayla R. Elliott, Yuxin Liu, Stephen D. Zucker   +5 more
wiley   +1 more source