Results 201 to 210 of about 104,547 (303)
Diagnostic Factors Associated with Sarcoidosis in Patients Referred for EBUS-TBNA Due to Mediastinal Lymphadenopathy. [PDF]
Zając P +4 more
europepmc +1 more source
ABSTRACT Abdominal tuberculosis (TB) is uncommon in Taiwan and frequently mimics malignancy or other infectious diseases due to nonspecific clinical manifestations, often leading to delayed diagnosis. We report a 72‐year‐old man who presented with fever, anorexia, weight loss, and epigastric discomfort.
Yi‐Lin Lin +2 more
wiley +1 more source
Chronic myeloid leukemia presenting with isolated central nervous system lymphoid blast crisis: A case report. [PDF]
Zarama-Valenzuela Á +3 more
europepmc +1 more source
ABSTRACT Mycoplasma pneumoniae (MP) is a common pediatric respiratory pathogen that can rarely present with extrapulmonary manifestations such as hepatic involvement. Recognition of hepatic dysfunction in this context is important for accurate diagnosis and timely therapy.
Robert J. Heins +2 more
wiley +1 more source
Clinical Images: Granulomatosis with polyangiitis mimicking cervical cancer
ACR Open Rheumatology, Volume 8, Issue 4, April 2026.
Haojie Xu +5 more
wiley +1 more source
ABSTRACT Tropheryma whipplei, traditionally linked to classic Whipple's disease with gastrointestinal involvement, is increasingly recognized as a cause of pneumonia. Reports of T. whipplei‐associated pneumonia progressing to respiratory failure with concurrent acute cardiac failure remain extremely rare.
Guisong Zhu +3 more
wiley +1 more source
ABSTRACT Juvenile Systemic Lupus Erythematosus (JSLE) is a rare and chronic multisystem autoimmune condition with an accelerated course compared with adult‐onset SLE. Its heterogeneity of presentation and overlap with infectious and inflammatory conditions frequently hinders diagnosis, especially in areas where tuberculosis is endemic.
Shafaq Nazia +5 more
wiley +1 more source
Looking Beyond the Surface: A Case of Shigella Enterocolitis in a Patient Presenting With Weakness and Substance Use. [PDF]
Lytle E, Le K, Le H.
europepmc +1 more source
ABSTRACT Rosai‐Dorfman disease is a rare non‐Langerhans cell histiocytic disorder. It is common in male children and young adults of African descent. It is classified into sporadic and familial types. The most common clinical presentation is massive bilateral cervical lymphadenopathy associated with constitutional symptoms. Histiocytic emperipolesis is
George Evele +2 more
wiley +1 more source
Atypical Presentation of Gangrenous Cholecystitis in a Patient With Diabetes Mellitus. [PDF]
Ahmad M +5 more
europepmc +1 more source

