Results 1 to 10 of about 584,998 (146)

Idiopathic Multicentric Castleman Disease Associated With Seronegative Erosive Chronic Polyarthritis: A Diagnostic Challenge [PDF]

Clin Case Rep
ABSTRACT Idiopathic multicentric Castleman disease can rarely present with systemic inflammation and erosive seronegative polyarthritis. Awareness of this association helps prevent misdiagnosis and ensures appropriate immunosuppressive management based on clinicopathological and immunohistochemical correlation.
Lo B, Kane B, Benjelloun F, Niang M, Kaïré I, Siddiki C, Razafimandimby A, Deme H, Dial C, Pouye A.   +9 more
europepmc   +2 more sources

Idiopathic Multicentric Castleman Disease With Severe Eosinophilia and Diffuse Centrilobular Nodule-A Rare Case Report. [PDF]

Case Rep Hematol
Rationale Idiopathic multicentric Castleman disease (iMCD), also known as angiofollicular lymph node hyperplasia, is a rare inflammatory lymphoproliferative disease with diverse clinical presentations. We report a rare case of iMCD accompanied by severe eosinophilia and diffuse centrilobular pulmonary nodules, which have rarely been previously ...
Li X, Li S, Zhao T, Xu B, Du X, Song X, Wang Y.   +6 more
europepmc   +2 more sources

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

Journal 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, Sri Aurobindo Prasad Das, Seema Rao, Samiran Nundy, Naimish N. Mehta   +4 more
doaj   +2 more sources

Castleman's Disease: Due to a Rare Intraabdominal Location

Forbes 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, Nursel Yurttutan, Betül Kızıldağ, Turgay Kara, Sezen Koçarslan   +4 more
doaj   +1 more source

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

Zaporožskij 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, N. M. Vdovina, H. I. Klymniuk, L. I. Omelchenko, T. A. Hridina, N. B. Matsiuk   +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

Zaporožskij 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, I. A. Lurin, V. V. Makarov, V. V. Nehoduiko, O. V. Buchnieva, S. V. Tertyshnyi, Y. V. Bunin   +6 more
doaj   +1 more source

POEMS syndrome: Update on diagnosis, risk‐stratification, and management

American Journal of Hematology, Volume 98, Issue 12, Page 1934-1950, December 2023., 2023
Abstract Disease Overview POEMS syndrome is a life‐threatening condition due to an underlying plasma cell neoplasm. The major criteria for the syndrome are polyradiculoneuropathy, clonal plasma cell disorder, sclerotic bone lesions, elevated vascular endothelial growth factor, and the presence of Castleman disease.
Angela Dispenzieri
wiley   +1 more source

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

Srpski 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, Krstić Svetlana, Subotić Dragan, Eminović Tatjana, Radojičić Jelena   +4 more
doaj   +1 more source

Transformation of HHV‐8‐negative idiopathic multicentric Castleman disease into diffuse large B‐cell lymphoma: A case report from Nepal

Clinical Case Reports, Volume 11, Issue 9, September 2023., 2023
Microscopic and Immunohistochemistry findings in Castleman Disease. Key Clinical Message Idiopathic Castleman disease transforming into Diffuse Large B‐cell Lymphoma has an aggressive course and can lead to mortality. Hence, early diagnosis and intervention are required.
Ashwini Gupta, Ayush Anand, Salman Haidar Hussain, Raju Shah, Rajesh Ranjan, Viplaw Subedi, Aastha Baral, Akshat Mishra, Anju Pradhan, Soniya Dulal   +9 more
wiley   +1 more source

Comprehensive Diagnosis and Management of POEMS Syndrome

HemaSphere, Volume 6, Issue 11, November 2022., 2022
Polyneuropathy Organomegaly, Endocrinopathy, Monoclonal protein and Skin changes syndrome is a rare multisystem condition with a range of manifestations which are often overlooked as trivial comorbidities, until their whole triggers the possibility of the diagnosis.
Shirley D'Sa, Jahanzaib Khwaja, Stephen Keddie, Ryan YS Keh, Duncan Smyth, Ruth Ronneberger, Suraiya Dubash, Suganya Sivabalasingham, Simon Wan, Chandrashekar Hoskote, Stephanie Baldeweg, Jonathan Sive, Michael P. Lunn   +12 more
wiley   +1 more source