Results 91 to 100 of about 8,688 (201)

A Comparison Study of Lymph Node Tuberculosis and Sarcoidosis Involvement to Facilitate Differential Diagnosis and to Establish a Predictive Score for Tuberculosis

Pathogens
Background: Tuberculosis (TB) and sarcoidosis are two common granulomatous diseases involving lymph nodes. Differential diagnosis is not always easy because pathogen demonstration in tuberculosis is not always possible and both diseases share clinical ...
Ellen Hoornaert, Halil Yildiz, Lucie Pothen, Julien De Greef, Olivier Gheysens, Alexandra Kozyreff, Diego Castanares-Zapatero, Jean Cyr Yombi   +7 more
doaj   +1 more source

Case Report: two cases of idiopathic plasmacytic lymphadenopathy subtype of idiopathic multicentric Castleman disease with xanthelasma palpebrum from a Canadian center

Frontiers in Hematology
BackgroundIdiopathic plasmacytic lymphadenopathy is a newly recognized subtype of idiopathic multicentric Castleman disease (iMCD-IPL) and often mimics IgG4-related disease (IgG4-RD).
Andrew A. Y. Chen, Vivian T. Yin, Paula Blanco, Mark Trinder, Richard I. Crawford, Richard I. Crawford, Ryan Henrie, Stephen Parkin, Nasreen Khalil, Mollie Carruthers, Lu Zhang, Luke Y. C. Chen, Luke Y. C. Chen   +12 more
doaj   +1 more source

Bone Marrow Negative Visceral Leishmaniasis in an Adolescent Male

Iranian Journal of Parasitology, 2013
Visceral Leishmaniasis or Kala Azar is endemic in certain regions of India. In endemic areas, the constella­tion of fever, progressive weight loss, weakness, pronounced splenomegaly, anemia, leukope­nia, and hypergammaglobulinemia is highly suggestive of
S Jetley, S Rana, S Khan, JS Zeeba, MJ Hassan, P Kapoor   +5 more
doaj   +2 more sources

Eosinophilic Fasciitis: A Review of Research and Therapeutic Possibilities

Journal of Education, Health and Sport
Introduction Eosinophilic fasciitis (EF) is a rare inflammatory disorder marked by elevated eosinophils in tissues and blood. Patients typically present with symptoms such as skin swelling, pain, and induration, which can be mistaken for other ...
Julia Biernikiewicz, Anna Wilewska, Bartosz Pomirski, Agata Pomirska, Milena Biernikiewicz, Konstanty Alabrudziński, Agnieszka Borowiec, Kinga Borowiec, Paulina Kwaśniewska, Patryk Graczyk   +9 more
doaj   +1 more source

[Hypergammaglobulinemia D syndrome].

Anales de medicina interna (Madrid, Spain : 1984), 2000
The hyperimmunoglobulinemia D syndrome is characterized by early onset of attacks of periodic fever and an elevated serum polyclonal Ig D (> 100 U/ml). Symptoms during attacks include joint involvements (arthralgia/arthritis), skin lesions, swollen lymph nodes, headache and abdominal complaints (vomiting, diarrhea and pain).
M, Medrano San Ildefonso, C, Bruscas Izu
openaire   +1 more source

Hypergammaglobulinemia and the anticardiolipin antibody test [PDF]

Arthritis & Rheumatism, 1989
T P, Hughes, P, Jones, M C, Rozenberg
openaire   +2 more sources

Rituximab-induced serum sickness: Not so uncommon

Indian Journal of Rheumatology, 2018
Vikramraj K Jain
doaj   +1 more source

Acute Liver Failure During Thyroid Storm With Autoimmune Hepatitis Overlap: A Rare Immunoendocrine-Hepatic Intersection. [PDF]

ACG Case Rep J
Pacheco Oliva JG, Meléndez Rodríguez N, Castellanos AJ, Sánchez AA, Sánchez MA.   +4 more
europepmc   +1 more source

Hypergammaglobulinemia [PDF]

, 2020
openaire   +1 more source

Severe Hyperferritinemia in Metabolic Dysfunction-Associated Steatotic Liver Disease With Normal Transferrin Saturation and Polyclonal Hypergammaglobulinemia Mimicking Iron Overload. [PDF]

Cureus
Ottu Para NK, Koshy G, Rab S.
europepmc   +1 more source