Results 161 to 170 of about 90,629 (291)

Appendiceal Crohn's Disease Manifesting as Appendiceal Malignancy: A Case Report and Review of the Literature

The Kaohsiung Journal of Medical Sciences, EarlyView.
Ming‐Jung Meng, Tai‐Di Chen, Puo‐Hsien Le, Chia‐Jung Kuo   +3 more
wiley   +1 more source

Targeting Immunologic Pathways in Eosinophilic Granulomatosis With Polyangiitis: Translating Emerging Evidence Into Clinical Practice

Allergy, EarlyView.
ABSTRACT Eosinophilic granulomatosis with polyangiitis (EGPA) is a rare and potentially life‐threatening systemic, inflammatory disease with multi‐organ manifestations, variable presentation and complex pathology. Multiple interconnected immunological pathways are implicated in EGPA pathology, including a type‐2 immune response driving predominantly ...
Harold Wilson‐Morkeh, Lior Seluk, Philipp Bosch, Carolina Aguiar, Jens Thiel, Bernhard Hellmich, Michael E. Wechsler, Salman Siddiqui   +7 more
wiley   +1 more source

Clinical updates of JAK inhibitors in cutaneous granulomatous diseases. [PDF]

Front Immunol
Gu J, He X, Lu B, Wang J, Chen K, Wang Q, Jian X, Huang C, Yu B.   +8 more
europepmc   +1 more source

Schistosomal appendicitis: a case series. [PDF]

J Surg Case Rep
Hijan EA, AlAli MN, Al-Darwish AS, Amer SM, Alasheikh M, AlRashed M, Aldeghaither SK, Essa MS.   +7 more
europepmc   +1 more source

Bleeding Disorders in Children With Genetic Diseases: A Narrative Review

Acta Paediatrica, EarlyView.
ABSTRACT Aim The lack of data on bleeding risk assessment in children with genetic diseases is concerning given their increased care needs and risk of haemorrhagic complications compared to the general population. Identification of haemostatic disorders is crucial for implementing preventive measures and mitigating bleeding risk.
Raphaelle Cagol, Mariam Sbeity Barakat, Marjolaine Willems, Tasnime Akbaraly, Biron‐Andreani Christine, Isabelle Diaz, Alexandre Theron   +6 more
wiley   +1 more source

Ulcerated necrobiosis lipoidica: clinical and histopathological presentation of two cases. [PDF]

An Bras Dermatol
Giriboni VM, Cortes LS, Terra SA, Abbade LPF.   +3 more
europepmc   +1 more source

Renal limited sarcoidosis presenting with non-caseating granulomatous interstitial nephritis in the absence of extrarenal manifestations: a case report and literature review. [PDF]

CEN Case Rep
Yanagisawa K, Takeuchi K, Wada Y, Saito G, Hanyuda M, Okawa H, Uchitsubo R, Kawamura S, Sakurabayashi S, Sano K, Motohashi T, Naito S, Aoyama T, Takeuchi Y.   +13 more
europepmc   +1 more source

Oral mucosal manifestations with identical mutations to the bone marrow in a patient with VEXAS syndrome

Rheumatology &Autoimmunity, EarlyView.
Lilian Vasaitis, Lena Blomstrand, Tatjana Pandzic, Miklos Gulyas, Panagiotis Baliakas, Viktor Ljungström   +5 more
wiley   +1 more source

Cutaneous non‐tuberculous mycobacterial infections: A retrospective study of 94 cases from Germany

JDDG: Journal der Deutschen Dermatologischen Gesellschaft, EarlyView.
Summary Background Cutaneous non‐tuberculous mycobacterial infections (NTM) remain a diagnostic and therapeutic challenge. The aim of this study was to characterize cutaneous NTM infections in Germany over a 24‐year‐period. Patients and Methods 73 patients with cutaneous NTM infections diagnosed at 17 different German University Hospitals from 2000 ...
Luisa Bopp, Nicolai Deresz, Henning Klapproth, Isabelle Suárez, Jonathan Jantsch, Mario Fabri, Esther von Stebut   +6 more
wiley   +1 more source

The diagnostic dilemma of idiopathic granulomatous mastitis with an emphasis on histopathologic findings. [PDF]

Diagn Pathol
Anousha K, Jahanbin B, Ardalan FA, Soleimani V, Azizi M, Rezvani A.   +5 more
europepmc   +1 more source