Results 71 to 80 of about 42,457 (287)

Langerhans cell histiocytosis in an adult patient

Vestnik Dermatologii i Venerologii, 2019
Aim: to present a clinical case of a rare dermatosis — Langerhans cell histiocytosis (LCH) in an adult patient.Materials and methods. A clinical and laboratory examination of a 64-year-old woman who had complained of rashes on the skin of the scalp, neck,
A. E. Karamova, V. V. Chikin, L. F. Znamenskaya, M. A. Nefedova, V. A. Mikhina, N. S. Battalova   +5 more
doaj   +1 more source

Emergence of cutaneous Rosai–Dorfman disease during immunosuppressive treatment of follicular B-cell lymphoma: A case report

SAGE Open Medical Case Reports, 2021
Background: Sinus histiocytosis with massive lymphadenopathy, also known as Rosai–Dorfman disease, is a rare proliferation of non-Langerhans histiocytes.
Sharon L Kipfer, Michael Samycia, Carolyn J Shiau   +2 more
doaj   +1 more source

Histiocytic Glomerulopathy With Noncrystalline Inclusion Associated With IgG-Kappa Plasma Cell Dyscrasia

Kidney Medicine, 2023
The kidney pathology of monoclonal gammopathy of renal significance varies greatly. In this report, we present a woman in her 20s with nephrotic syndrome and monoclonal immunoglobulin G kappa (serum and urine) without diabetes.
Ai Katsuma, Masahiro Okabe, Hiroyuki Ueda, Takashi Ehara, Yutaka Yamaguchi, Yoichi Miyazaki, Takashi Yokoo   +6 more
doaj   +1 more source

Disseminated cutaneous gout: a rare manifestation of a common disease [PDF]

, 2020
Disseminated cutaneous gout is a rare atypical cutaneous manifestation of gout in which widespread dermal and subcutaneous tophi develop at extra-articular body sites.
Adler, Brandon L, Crew, Ashley, DeClerck, Brittney, Guzman, Ruben, Peng, David   +4 more
core  

Therapeutic efficacy of favipiravir against Bourbon virus in mice [PDF]

, 2019
Bourbon virus (BRBV) is an emerging tick-borne RNA virus in the orthomyxoviridae family that was discovered in 2014. Although fatal human cases of BRBV have been described, little is known about its pathogenesis, and no antiviral therapies or vaccines ...
Bailey, Thomas, Boon, Adrianus C. M., Bricker, Traci L, Diamond, Michael S, Gounder, Anshu P, Jagger, Brett W, Janowski, Andrew B, Kwon, Jennie H, Shafiuddin, Md., Wang, David, Williams, Graham D, Zhao, Guoyan   +11 more
core   +3 more sources

Primary splenic T-cell/histiocyte-rich B-cell lymphoma in a patient with recurrent hairy cell leukemia: a case report [PDF]

, 2022
Tagrid Younes Ahmad, Hasan Nabil Al Houri, Sami Jomaa, Wisam Hikmat Assad, Sarah Zaher Addeen   +4 more
openalex   +1 more source

A Refractory Leg Skin Ulcer Associated With Multiple Myeloma Successfully Treated With Plasma Exchange, Lenalidomide, and Dexamethasone

JEADV Clinical Practice, EarlyView.
ABSTRACT Multiple myeloma (MM) is a malignant plasma cell disorder that primarily presents with CRAB symptoms (calcium elevation, renal failure, anemia, and bone abnormalities). In rare cases, MM manifests with systemic complications like skin ulcers, which present management challenges. Here, we report a 78‐year‐old Japanese man with MM and refractory
Naoko Hattori, Yutaka Kuwatsuka, Tomoka Waseda, Daisuke Ehara, Koji Ando, Hiroyuki Murota   +5 more
wiley   +1 more source

Xanthogranulomatous Oophoritis- A Rare Inflammatory Lesion [PDF]

Journal of Krishna Institute of Medical Sciences University, 2013
Xanthogranulomatous inflammation is a specialform of chronic inflammation that is destruc-tive of affected organ. Xanthogranulomatous in-flammation of ovary and fallopian tube is an un-common entity and it is usually known to oc-cur in the kidney and ...
Mahesh H Karigoudar, Anirudha V Kushtagi, Rashmi M Karigoudar, Anilkumar Sirasagi1   +3 more
doaj  

Primary unifocal thymic Rosai-Dorfman disease: an extremely rare challenge in diagnostic practice

Journal of Cardiothoracic Surgery, 2023
Rosai-Dorfman disease (RDD) is currently considered a group of neoplastic diseases of unknown etiology, with monoclonal proliferation of histiocytes, showing unique histopathologic features and varying clinical presentation.
Qian Liu, Fengxiang Liao, Yong Liu, Yang Cheng, Chubo Qi   +4 more
doaj   +1 more source

histiocytic Necrotizing Lymphadenitis

Apollo Medicine, 2006
We are presenting a case of histiocytic necrotizing lymphadenitis (Kikuchi disease), which is characterized by involvement of lymph nodes, skin, liver and spleen. A 21-year-old girl presented with 27 days history of prolonged fever, left cervical painless lymphadenitis and maculo-papular skin rashes.
Vijay Kumar Aneja, Deepshikha Arora, S. Chatterjee   +2 more
openaire   +1 more source