Results 151 to 160 of about 13,533,670 (328)

Essential Thrombocythemia's Role in the Complex Landscape of Vasculitis: A Case Report

open access: yesClinical Case Reports, Volume 13, Issue 10, October 2025.
ABSTRACT Peripheral gangrenes have been sporadically documented as the initial presentation of essential thrombocythemia (ET), as exemplified in the preceding case reports. Nevertheless, the prevalence of vasculitis‐induced skin problems as the primary indication of ET has not been extensively examined.
Mohammad Reza Jafari Nakhjavani   +8 more
wiley   +1 more source

Pregnancy in Takayasu Arteritis: A Case Report of Successful Pregnancy in a Large Aortic Aneurysm

open access: yesClinical Case Reports, Volume 13, Issue 10, October 2025.
ABSTRACT A 29‐year‐old primigravida woman with a gestational age of 19 weeks visited in the cardio‐obstetrics clinic for hypertension. Physical examination revealed auscultated systolic and diastolic murmurs in the second right intercostal space. Transthoracic echocardiography (TTE) showed severe left ventricle (LV) enlargement with mild systolic ...
Mona Yadollahi   +5 more
wiley   +1 more source

764 A Study on the Outcome of Direct Coombs Test (DCT) Positive Neonates [PDF]

open access: bronze, 2012
K. Upatissa   +2 more
openalex   +1 more source

Roxadustat for ESA‐Hyporesponsive Renal Anemia in a 13‐Year‐Old on Hemodialysis: Case Report and Mini‐Review

open access: yesClinical Case Reports, Volume 13, Issue 10, October 2025.
Changes in hemoglobin and iron metabolism parameters during Roxadustat treatment in a 13‐year‐old dialysis patient. ABSTRACT Anemia is the most common complication of end‐stage renal disease (ESRD). While erythropoiesis‐stimulating agents (ESA) have improved treatment outcomes, some patients exhibit intolerance or hyporesponsiveness.
Meng Zhang   +3 more
wiley   +1 more source

Clinical and Genetic Analysis of Dehydrated Hereditary Stomatocytosis: A Case Report

open access: yesClinical Case Reports, Volume 13, Issue 10, October 2025.
ABSTRACT Dehydrated hereditary stomatocytosis (DHS) is a rare autosomal dominant hemolytic anemia caused by abnormal erythrocyte ion permeability, most often due to PIEZO1 mutations. We report the case of a 15‐year‐old male with elevated indirect bilirubin and mild anemia.
Chen Ming, Shiyuan Wu, Rui Pan
wiley   +1 more source

Pediatric Gastric Adenocarcinoma in the Setting of Celiac Disease: A Rare and Insightful Case Report

open access: yesClinical Case Reports, Volume 13, Issue 10, October 2025.
ABSTRACT Gastric adenocarcinoma is exceptionally rare in children, often presenting with nonspecific gastrointestinal (GI) symptoms. This case highlights the importance of considering malignancy in pediatric patients with celiac disease and poor dietary adherence, as complications like gastric adenocarcinoma can arise.
Mahsa Rouhafshari   +4 more
wiley   +1 more source

Hepatogastric Fistula as a Rare Complication of Pyogenic Liver Abscess: A Case Report

open access: yesClinical Case Reports, Volume 13, Issue 10, October 2025.
ABSTRACT Hepatogastric fistula is a rare complication of pyogenic liver abscess. We report an 18‐year‐old male with 3 weeks of fever, melena, and epigastric discomfort. Ultrasound showed a contracted gallbladder with wall thickening and sludge without cholelithiasis.
Mohammad Kazem Amirbeigy   +3 more
wiley   +1 more source

Alterations of erythropoiesis in Covid-19 patients: prevalence of positive Coombs tests and iron metabolism [PDF]

open access: gold, 2023
Léa Schmitz   +11 more
openalex   +1 more source

Autoimmune hemolytic anemia in children

open access: yesPediatric Hematology Oncology Journal
Autoimmune hemolytic anaemia (AIHA) is an uncommon cause of antibody-induced hemolytic anemia in children. It is divided into three categories: warm AIHA, cold antibody AIHA and paroxysmal cold hemoglobinuria. The diagnostic work-up typically begins with
Dinesh Chandra   +3 more
doaj   +1 more source

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