Results 101 to 110 of about 3,791 (140)

Association of Autoimmune Diseases With Pancreatic Cancer: A Nationwide Follow‐Up Study From Sweden

Cancer Medicine, Volume 15, Issue 3, March 2026.
Graphic abstract illustrating the nationwide cohort design used to investigate the association between autoimmune diseases and the risk of pancreatic cancer in Sweden. ABSTRACT Background The incidence of pancreatic cancer (PC) and autoimmune diseases (ADs) has been increasing worldwide.
Jiarong Gu, Yuhong Zhang, Kristina Sundquist, Jan Sundquist, Huifang Yang, Wenhua Ling, Xinjun Li   +6 more
wiley   +1 more source

Editorial: Interstitial Lung Disease Around the World

Frontiers in Medicine, 2022
Marlies Wijsenbeek, Joyce S. Lee, Zarir Udwadia, Michael Kreuter, Michael Kreuter   +4 more
doaj   +1 more source

A Case of Intermittent Fever a Decade After Renal Transplantation

Clinical Case Reports, Volume 14, Issue 3, March 2026.
ABSTRACT Disseminated histoplasmosis is a potentially serious complication after organ transplantation; however, its occurrence is rare, even in endemic regions. Diagnosis can be challenging, particularly in patients with nonspecific symptoms such as intermittent fever or lethargy.
Merazul Islam Ony, Baris Afsar, Bahar Bastani   +2 more
wiley   +1 more source

Abdominal Cocoon Syndrome With Greater Omental Hypoplasia: A Rare Anatomical Insight and Diagnostic Challenge

Clinical Case Reports, Volume 14, Issue 3, March 2026.
ABSTRACT Abdominal cocoon syndrome, or idiopathic sclerosing encapsulating peritonitis (SEP), is an uncommon cause of small bowel obstruction marked by the encasement of bowel loops within a dense fibrocollagenous membrane. Due to its rarity and nonspecific presentation, diagnosis is frequently delayed, particularly in patients without prior abdominal ...
Sohrab Sayyadi, Keihan Shabankhani, Mohammad Mahdi Sargazi Moghaddam, Seyed Mohammad Sakhaei, Mina Alvandipour, Seyed Muhammad Mehdi Ghaffari Hamedani, Hossein Farsavian, Mohammad Javad Najafi   +7 more
wiley   +1 more source

Paucibacillary Pleural Tuberculosis Presenting as Subpleural Nodules: A Diagnostic Challenge With Negative PCR and Smear Tests

Clinical Case Reports, Volume 14, Issue 3, March 2026.
ABSTRACT Pleural tuberculosis is a common manifestation of extrapulmonary tuberculosis; however, its diagnosis remains challenging in paucibacillary disease, where clinical presentation may be atypical and microbiological tests frequently yield negative results.
Omar Al Ayoubi, Mohammad Alaa Aldakak, Bassel Ibrahim, Raneem Ahmad, Youness Souleiman   +4 more
wiley   +1 more source

Non‐Specific Interstitial Pneumonia in Anti‐Jo1 Synthetase Syndrome With Probable Gougerot Syndrome: A Case Report

Clinical Case Reports, Volume 14, Issue 3, March 2026.
ABSTRACT Anti‐synthetase syndrome (ASS) is a rare autoimmune disorder of idiopathic inflammatory myopathy spectrum, characterized by the presence of aminoacyl‐tRNA synthetase antibodies, most commonly anti‐Jo‐1. Clinically presents with interstitial lung disease (ILD), myositis, and arthritis, and may be confused with other autoimmune conditions such ...
Ali Gohar, Ozaire Mohammad, Ruman Shahzad, Fatima Arshad, Abdul Rehman Shahid Khan, Hamad Qayyum, Joham Ajmal, Muhammad Husnain Ahmad   +7 more
wiley   +1 more source

Cutaneous Leishmaniasis in High‐Altitude: A Case Report From Nepal

Clinical Case Reports, Volume 14, Issue 3, March 2026.
ABSTRACT Leishmaniasis is a parasitic infection caused by Leishmania and spread by the bite of a sandfly, most commonly Phlebotomus. Among the three subtypes of Leishmaniasis, cutaneous leishmaniasis is the most common form. Visceral Leishmaniasis is common in Nepal whereas few cases of cutaneous leishmaniasis have been reported in migrant Nepalese ...
Eliz Aryal, Rohan Sapkota, Sunny Shrestha, Arika Baral, Santosh Sapkota, Mandish Prasad Phuyal   +5 more
wiley   +1 more source

Clinical, biological and cytometric characteristics of two patients with a homozygous A91V PRF1 mutation

Clinical &Translational Immunology, Volume 15, Issue 3, March 2026.
Familial haemophagocytic lymphohistiocytosis (FHL) is a rare, inherited granzyme–perforin system defect that predisposes individuals to haemophagocytic lymphohistiocytosis. This article presents two original case reports of FHL type 2, along with a comprehensive literature review. Together, these elements aim to enhance the current understanding of FHL
Nicolas Perrard, Claire Poggi, Sébastien Sanges, Bruno Lemarchant, Wadih Abou Chahlah, Louis Terriou, Stéphanie Delangue, Jacques Trauet, Myriam Labalette, Eric Hachulla, Despina Moshous, Guillaume Lefevre, David Launay   +12 more
wiley   +1 more source

Distinguishing lung cancer from atypical tuberculosis: Deep transfer learning and imaging omics features

Journal of Intelligent Medicine, Volume 3, Issue 1, Page 69-80, March 2026.
The 3D‐ResNet model demonstrates superior discriminative power in differentiating lung cancer from atypical tuberculosis by leveraging deep omics features derived from volumetric lung cancer imaging, outperforming conventional clinical and radiomic analyses.
Yi Wu, Siyi Li, Zhiping Long, Yanjie Jia, Yue Yu, Bing Pei, Heli Yuan, Yuhua Hao, Zhiyun Jiang, Lei Cao, Kezheng Wang, Fan Wang   +11 more
wiley   +1 more source

Successful Treatment of Paediatric Necrobiosis Lipoidica With Baricitinib

JEADV Clinical Practice, Volume 5, Issue 1, Page 246-249, March 2026.
ABSTRACT Necrobiosis lipoidica (NL) is a rare, chronic granulomatous condition that typically presents as sharply demarcated plaques with telangiectasia and atrophic centres. Paediatric cases are uncommon, and treatment options often fail to address refractory cases.
P. Simões Farinha, M. J. Paiva‐Lopes
wiley   +1 more source