Results 71 to 80 of about 25,153 (346)

Primary tibial bone involvement in Rosai Dorfman Disease treated with surgery and radiotherapy; case report and literature review

Journal of Orthopaedic Reports
Rosai-Dorfman disease is a rare benign disease that is characterized by over-production and accumulation of white blood cells, known as (histiocytes) in the lymph nodes (nodal) or any other areas of the body (extranodal). It usually presents as painless,
Abdullah F. Alotaibi, Talal Alrawaf, Osama Alshaya, Hassan Sawan, Muath Aljufayr   +4 more
doaj   +1 more source

Successful Treatment of Paediatric Necrobiosis Lipoidica With Baricitinib

JEADV Clinical Practice, EarlyView.
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

Langerhans cell histiocytosis: current concepts in dentistry and case report [PDF]

, 2016
Langerhans cell histiocytosis (LCH), which is a rare granulomatous pediatric disease of unknown etiology, is characterized by the idiopathic proliferation and accumulation of abnormal and clonal Langerhans cells or their ...
Alejo-Gonzalez, Francisco, Garrocho Rangel, Arturo, Pozos Guillén, Amaury de Jesús, Ramos-Gutierrez, Efraín, Ruiz Rodríguez, Socorro   +4 more
core  

Langerhans´cell histiocytosis [PDF]

, 2014
La histiocitosis de células de Langerhans (HCL), anteriormente conocida como histiocitosis X, es una enfermedad poco frecuente caracterizada por la acumulación y proliferación de histiocitos, eosinófilos y células de Langerhans, con inclusión de gránulos
Casanovas, A., Elena, G., Rosso, Diego
core   +1 more source

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

Benign histiocyte-rich pseudotumor in post treatment mediastinal Hodgkin's lymphoma

Radiology Case Reports, 2020
Benign xanthomatous pseudotumors are rare, mass forming lesions composed of lipid laden histiocytes and tumor necrosis following chemotherapy.We present a rare case of young 36 year old male with primary mediastinal Hodgkin's lymphoma who developed ...
Yash Dilip Nilak, MBBS, DA, MRCP, Anjumara Nilak, MBBS, DMRE, DNB(Rad), MMED, FRCR, Salim Shafeek, MD FRCP FRCP(Ed) FRCPath(Haem), Dr. Zbigniew Rudzki, Joanne Chapman, BM, FRCPath, PGCE   +4 more
doaj   +1 more source

T-Cell/Histiocyte-Rich Large B-Cell Lymphoma of the Thyroid

Experimental Hematology & Oncology, 2013
T-cell/histiocyte-rich large B-cell lymphoma (THRLBCL) is a rare subtype of diffuse large B-cell lymphoma, and has been reported to mainly affect lymph nodes with advanced Ann Arbor stage.
S. Ichikawa, Yasuaki Watanabe, Kei Saito, J. Kimura, R. Ichinohasama, H. Harigae   +5 more
semanticscholar   +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

An unusual case of intertrigo in an adult caused by purely cutaneous Langerhans cell histiocytosis [PDF]

, 2016
We report a case of persistent intertrigo in an adult, eventually diagnosed as cutaneous Langerhans cell histiocytosis (LCH). It is known that LCH has a predilection for intertriginous areas, however purely cutaneous disease as in our case, is uncommon ...
Baldacchino, Godfrey, Betts, Alexandra, Boffa, Michael J., Gatt, Alex   +3 more
core  

Cavoatrial Bypass for Cardiac Complications From Rosai-Dorfman Disease

Annals of Thoracic Surgery Short Reports
Rosai-Dorfman disease (RDD) is a nonmalignant disease of histiocyte proliferation. RDD usually presents with painless cervical lymphadenopathy, although extranodal involvement can occur. Cardiac involvement was reported in
Quynh Nguyen, MD, Rachel Bourke, MD, Richard W. Gilbert, MD, Graziano Oldani, MD, Jong Moo Kim, MD, Andrew Lytle, MD, Richard C. Cook, MD, Hilary P. Grocott, MD, Joel Price, MD, MPH   +8 more
doaj   +1 more source