Results 1 to 10 of about 623,470 (191)

Retroperitoneal Castleman disease masquerading as a pancreatic neoplasm: a case report and review of the literature [PDF]

open access: yesJournal of Medical Case Reports
Background Castleman disease (CD) is a rare lymphoproliferative disorder of unclear etiology, often presenting as an asymptomatic, incidentally detected mass.
Sanket Solanki   +4 more
doaj   +2 more sources

Castleman's Disease: Due to a Rare Intraabdominal Location

open access: yesForbes Tıp Dergisi, 2021
Castleman disease (CD) is a rare benign disease with unknown etiology. It is also called angiofollicular lymph node hyperplasia, giant lymph node hyperplasia, lymph node hamartoma, benign giant lymphoma.
Mehmet Cihan Karacaoğlu   +4 more
doaj   +1 more source

Lymphoproliferative disorder – Castleman’s disease with early childhood-onset in a child (a clinical case)

open access: yesZaporožskij Medicinskij Žurnal, 2022
Castleman’s disease (angiofollicular lymphoma, giant lymph node hyperplasia, Castleman’s pseudotumor) is an understudied orphan lymphoproliferative disease with a long period of asymptomatic course and a high risk of malignancy, and variability of its ...
O. M. Mukvich   +5 more
doaj   +1 more source

A clinical case of gunshot shrapnel penetrating wound of the chest with injury to the inferior vena cava with migration of a foreign body along the blood stream

open access: yesZaporožskij Medicinskij Žurnal, 2022
Castleman’s disease (angiofollicular lymphoma, giant lymph node hyperplasia, Castleman’s pseudotumor) is an understudied orphan lymphoproliferative disease with a long period of asymptomatic course and a high risk of malignancy, and variability of its ...
V. I. Tsumbaliuk   +6 more
doaj   +1 more source

Incidentally detected Castleman disease in a patient with allergic rhinosinu sitis [PDF]

open access: yesSrpski Arhiv za Celokupno Lekarstvo, 2008
INTRODUCTION Castleman disease was for the first time described in 1956 as a mediastinal tumour mass. Etiology of this disease is still unknown. The disease can be solitary and multicentric or rarely of a mixed type.
Stojšić Jelena   +4 more
doaj   +1 more source

Castleman’s Disease Intra Parotid, a Case Report and Literature Review [PDF]

open access: yesJournal of Dentistry, 2021
Castleman’s disease (CD), otherwise known as angiofollicular lymph node hyperplasia, is a rare, poorly understood disorder, which often occurs in a mediastinum. Involvement of parotid gland is a considerably infrequent event. We present a 15-year-old boy
Neda Kardouni Khoozestani   +3 more
doaj  

Castleman's disease, an unusual presentation

open access: yesJournal of Marine Medical Society, 2015
Presentation with intra-abdominal lymphadenopathy comes with a wide range of differentials, usually metastasis from regional organs, tuberculosis and lymphomas. But sometimes they surprise us with a histopathological diagnosis of Castleman's disease (CD).
Shital Munde   +6 more
doaj   +1 more source

Variant of plasmablastic microlymphoma in Castleman disease: a case report and review of the literature

open access: yesItalian Journal of Medicine, 2018
Castleman disease (CD) is a rare lymphoproliferative disorder also known as angiofollicular lymph node hyperplasia or giant lymph node hyperplasia. CD can be unicentric CD (UCD) or multicentric CD (MCD). MCD affects more than one group of lymph nodes and/
Nathan Artom   +10 more
doaj   +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

Doença de Castleman hialino-vascular do mediastino

open access: yesRevista Portuguesa de Pneumologia, 2000
RESUMO: A doença de Castleman ou hiperplasia angiofolicular dos gânglios linfáticos, é uma entidade pouco frequente e de origem desconhecida. Dois padrões histológicos distintos foram descritos: o tipo hialinovascular e o plasmo-celular.
Ana Paula Martins, Fernando Rocha
doaj   +1 more source

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