Results 51 to 60 of about 13,750 (216)

Multicentric Castleman's disease: a case report [PDF]

open access: yes, 2007
Castleman's disease is a clinicopathological entity associated with lymphoproliferation. We report a case of a 71 year old gentleman who was initially clinically suspected to have lymphoma (owing to clinical features at presentation), but was later ...
Brian F Menezes   +11 more
core   +2 more sources

SUBMANDIBULAR CASTLEMAN'S DISEASE

open access: yesInternational Journal of Clinical Practice, 2002
SUMMARYCastleman's disease is a rare benign lymphoid tumour of unknown aetiology, which usually appears as a solitary mediastinal mass. We report an unusual case of Castleman's disease, an asymptomatic submandibular mass in the lower jaw, and we discuss the computed tomography appearance.
S C, Chan   +5 more
openaire   +2 more sources

Refractory Castleman's Disease

open access: yesHematology, 1998
Angiofollicular lymph node hyperplasia is an uncommon low-grade lymphoproliferative disorder first described by Castleman. It is typically asymptomatic with diagnosis incidentally made in young males on chest radiology. Biopsy, in 90% of cases, shows the hyaline vascular variant.
P, Jacobs, L, Wood, V, Jogessar
openaire   +2 more sources

Intrathoracic Castleman disease

open access: yesTURKISH JOURNAL OF MEDICAL SCIENCES, 2014
To analyze patients with Castleman disease who were diagnosed by surgery.We retrospectively investigated the postoperative pathological records of operations performed between January 1992 and December 2012 in our hospital. Files of 19 patients with the diagnosis of Castleman disease were analyzed.There were 13 male and 6 female patients with a mean ...
Karaoğlanoğlu, NURETTİN   +6 more
openaire   +3 more sources

Immunophenotypic characteristics of plasma cells in POEMS syndrome

open access: yesCytometry Part B: Clinical Cytometry, EarlyView.
Abstract To analyze the immunophenotypic characteristics of plasma cells in patients with polyneuropathy, organomegaly, endocrinopathy, myeloma protein, and skin changes (POEMS) syndrome. This retrospective study included patients with POEMS syndrome hospitalized in the Department of Hematology, Huashan Hospital, from September 2017 to August 2025 ...
Zhenhua Wang   +6 more
wiley   +1 more source

Possible roles of Epstein-Barr virus in Castleman disease

open access: yesJournal of Cardiothoracic Surgery, 2009
Background Complete resection seemed to be curative in patients with Castleman disease of any location but the disease is likely to be reactive in its pathogenesis. The relation between Epstein-Barr virus and Castleman disease has not been elucidated. We
Liu Hung-Chang   +3 more
doaj   +1 more source

Unicentric mixed variant castleman disease associated with intrabronchial plasmacytoma. [PDF]

open access: yes, 2014
Castleman disease (CD), described as a heterogeneous lymphoproliferative disorder, can be divided into different subtypes according to clinical appearance (unicentric and multicentric form) and histopathological features (hyaline vascular, plasma cell ...
A Carbone   +42 more
core   +1 more source

Upper Airway Obstruction due to Kaposi Sarcoma—Presenting Sign of HIV: Case Report and Review

open access: yesThe Laryngoscope, EarlyView.
This study presents a case of undiagnosed HIV presenting with Kaposi sarcoma (KS) of the head and neck with acute upper airway obstruction (UAO) and provides an updated scoping literature review to examine the patient characteristics, lesion characteristics, interventions, and outcomes of KS cases with UAO from the pharynx, larynx, and/or trachea.
Zachary A. Wykoff   +3 more
wiley   +1 more source

A Rare Lymphoproliferative Disease: Castleman Disease

open access: yesTurkish Journal of Hematology, 2021
Castleman disease is a rare lymphoproliferative disease also known as angiofollicular lymph node hyperplasia. It is classified as hyaline vascular and plasmacytic variants histologically but characteristics of both types can coexist.
Eren Gündüz   +3 more
doaj   +1 more source

Oral Angiolymphoid Hyperplasia With Eosinophilia Exhibiting Cutaneous‐Type Histopathologic Features: Clinical Regression Following Hormonal Withdrawal and a 50‐Year Review

open access: yesJournal of Cutaneous Pathology, EarlyView.
Case report of a 30‐year‐old female. Asymptomatic, red‐purple hyperplastic lesion extending from teeth 21 to 25, with bleeding upon manipulation. Differential diagnosis included: inflammatory gingival hyperplasia, plasma cell gingivitis, leukemia, and Wegener's granulomatosis.
Pedro Vinícius Santos de Jesus   +8 more
wiley   +1 more source

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