Results 101 to 110 of about 45,305 (223)

Miliary Tuberculosis With Immune Thrombocytopenia in 50‐Year‐Old Ethiopian Woman: A Case Report and Brief Review of Literature

Clinical Case Reports, Volume 14, Issue 2, February 2026.
Diffuse petechiae and non‐palpable purpura (lower extremities below knee, admission photo). ABSTRACT Immune thrombocytopenia (ITP) is a rare but recognized hematologic complication of tuberculosis (TB), particularly miliary TB. We present a case of a 50‐year‐old female with severe thrombocytopenia and hemorrhagic manifestations secondary to miliary TB.
Hayatu Awel Abdela, Tamirat Godebo Woyimo, Ragasa Getachew Bayisa, Sisay Tagese Tafese   +3 more
wiley   +1 more source

Chiari I Malformation and Intramedullary Hemorrhage in a Female Patient with Klippel Trenaunay Syndrome: A Rare Case Report Study [PDF]

International Journal of Caring Sciences
Chiari I Malformation and Intramedullary Hemorrhage in a Female Patient with Klippel Trenaunay Syndrome: A Rare Case Report ...
Kalliopi Magounaki, Emmanouil Kalafatis, Dimitris Stergiou, Maria Tzaki, Dionysios Vekios, Aggelos Papakalos and Ioannis Kyriazis   +5 more
doaj  

Schistosomiasis with pericardial effusion

European Journal of Case Reports in Internal Medicine
Schistosomiasis, caused by parasitic flatworms of the genus Schistosoma, is endemic in many areas of the world. We report the case of a young male patient presenting with persistent fever, abdominal pain, vomiting and diarrhoea, with travel history to Al
Elaf Khalid Bajameel, Arifa Jamal, Asem Osama Banjar, Khalid Mohammed Alqahtani, Noura Babikir Ahmed Elsheikh, Arwa Hussain Alkhuraim   +5 more
doaj   +1 more source

Hepatosplenic schistosomiasis in field-based studies: a combined clinical and sonographic definition

Memorias do Instituto Oswaldo Cruz, 2001
A combined clinical and sonographic classification of hepatosplenic schistosomiasis mansoni to be used in field-based studies is proposed herein. Seven hundred forty one individuals out of 892 (83%), living in an area endemic for schistosomiasis in ...
José Roberto Lambertucci, Gláucia Fernandes Cota, Rogério Augusto Pinto-Silva, José Carlos Serufo, Rogério Gerspacher-Lara, Sandra Costa Drummond, Carlos Maurício Antunes, Vandack Nobre, Abdunnabi Rayes   +8 more
doaj   +1 more source

Bilateral Ulcers in Protothecosis: A Diagnostic Challenge

International Journal of Dermatology, EarlyView.
Waratchaya Panjapakkul, Charussri Leeyaphan, Penvadee Pattanaprichakul, Kanchalit Thanomkitti, Pattriya Jirawattanadon   +4 more
wiley   +1 more source

A Case Report on Disseminated Mycobacterium avium Complex Infection in an Otherwise Healthy Individual—A Diagnostic Challenge

Clinical Case Reports, Volume 14, Issue 2, February 2026.
ABSTRACT Disseminated Mycobacterium avium complex (MAC) infection can mimic tuberculosis (TB) in immunocompetent individuals, leading to diagnostic and therapeutic challenges. Clinicians should consider nontuberculous mycobacteria (NTM) in patients unresponsive to anti‐tubercular therapy (ATT), especially in endemic regions.
Abdulla Bin Hridoy, Shadman Newaz, Moontasir Ahmed, Jannat Ara Tina, Supritom Sarker, Anika Tabassum, Mohammad Zakaria Al‐Aziz, Md. Robed Amin   +7 more
wiley   +1 more source

Auer Rod‐Like Inclusions in Chronic Lymphocytic Leukemia: A Case Report

Clinical Case Reports, Volume 14, Issue 2, February 2026.
ABSTRACT Auer rod‐like inclusions may occasionally be observed in chronic lymphocytic leukemia. Their recognition on peripheral smear highlights the importance of meticulous morphology assessment when comprehensive hematologic testing cannot be performed.
Tingting Zhang, Linjun Xie
wiley   +1 more source

hepatosplenomegaly

Citation: 'hepatosplenomegaly' in the IUPAC Compendium of Chemical Terminology, 5th ed.; International Union of Pure and Applied Chemistry; 2025. Online version 5.0.0, 2025. 10.1351/goldbook.10793 • License: The IUPAC Gold Book is licensed under Creative Commons Attribution-ShareAlike CC BY-SA 4.0 International for individual terms.
openaire   +1 more source

Adult‐Onset Still's Disease(AOSD) With Features Suggestive of Macrophages Activation Syndrome in Young Female: A Rare Case Report From Nepal

Clinical Case Reports, Volume 14, Issue 2, February 2026.
ABSTRACT Adult‐onset Still's disease (AOSD) is a rare, multisystem autoinflammatory disorder characterized by a classic triad of fever, evanescent rash, and arthritis with diagnostic challenges. We present a case of a previously healthy 22‐year‐old Nepalese female presented with a 1.5‐month history of progressive bilateral lower limb edema and a 13‐day
Sushil Silwal, Krishan Khang Mandal, Gaurav Parajuli, Krishna Adhikari   +3 more
wiley   +1 more source

Hepatosplenomegaly [PDF]

, 2020
K. Gupta, P. Carmichael, A. Zumla
openaire   +2 more sources