Results 111 to 120 of about 9,327,495 (300)
Cronkhite–Canada Syndrome With Multiple Mesenteric Lymphadenopathy: A Case Report
ABSTRACT Cronkhite–Canada syndrome (CCS) is a rare nonhereditary disorder characterized by multiple gastrointestinal polyps and ectodermal changes. The mortality rate can reach up to 50% in patients with delayed diagnosis or inadequate treatment. A 78‐year‐old Japanese woman presented with diarrhea as the primary complaint.
Takashi Nishino +3 more
wiley +1 more source
Castlemans Disease- A Case Report
Castlemans disease(CD) is a heterogeneous group of lymphoproliferative disorders of uncertain cause presenting with lymphadenopathy. It is histologically and prognostically distinct from malignant lymph-node hyperplasia.
Md. Ismail Patwary +5 more
doaj +1 more source
Key Clinical Message Idiopathic multicentric Castleman disease (iMCD) is challenging to diagnose due to clinical similarities with other conditions, such as Still's disease.
Magdalena Strach +3 more
doaj +1 more source
n-3系脂肪散を強化した食事療法が有効と考えられた肺気腫の一例 [PDF]
An effective treatment for the advanced stages of chronic obstructive pulmonary disease (COPD) has not been established yet. We report our recent experience of one patient with pulmonary emphysema treated by dietary supplementation of n-3 fatty acid for ...
Ashida, Kozo +7 more
core +1 more source
BACKGROUND Patients with multicentric Castleman disease (MCD) who are negative for human immunodeficiency virus and human herpesvirus 8 are considered to have idiopathic MCD (iMCD).
Li Yu +20 more
semanticscholar +1 more source
Diagnostic challenges in patients with Castleman disease, a single center experience from Hungary
Castleman disease is a rare and atypical lymphoproliferative disorder characterized by diverse clinical manifestations. It has both unicentric and multicentric forms, the latter with further subdivisions, i.e., human herpesvirus 8-associated and ...
Boglárka Brúgós +6 more
doaj +1 more source
Hodgkin Lymphoma and Castleman Disease: When One Blood Disease Can Hide Another
We describe a rare case of Castleman disease associated de novo with Hodgkin lymphoma. The incidence of Castleman disease is rare; only a few studies have described it in de novo association with Hodgkin lymphoma. The patient described here complained of
L. Filliatre-Clement +4 more
doaj +1 more source
Recurrent PDGFRB mutations in unicentric Castleman disease
Castleman disease (CD) is a rare heterogeneous group of lymphoproliferative disorders that share common lymph node histopathological features [1, 2]. It can be classified into unicentric CD (UCD), HHV-8-positive multicentric CD (MCD) and HHV-8-negative ...
Zhaoming Li +26 more
semanticscholar +1 more source
A rare case report of hyaline-vascular type Castleman disease in the presacral region
Castleman disease (CD), also known as giant lymph node hyperplasia or angiofollicular lymph node hyperplasia, is a rare and indeterminate group of chronic lymphoproliferative disorders.
Long Chang +4 more
doaj +1 more source
Spatial Transcriptomics of Patients With Kaposi Sarcoma Identifies Mechanisms of Immune Evasion
ABSTRACT To identify the cell types that are infected with KSHV and the immune interactions in Kaposi sarcoma (KS) lesions, we performed spatial transcriptomics with seven KS skin tumors. We used a single‐cell RNA‐sequencing reference data set from healthy skin donors with a method to conduct spatially informed cell‐type deconvolution for spatial ...
Bahman Afsari +8 more
wiley +1 more source

