Results 81 to 90 of about 25,001,430 (174)

Multiple capillary hemangiomas: A distinctive lesion of multicentric Castleman's disease and POEMS syndrome [PDF]

, 2008
A diagnosed case of Castleman′s disease, proven by biopsy from enlarged inguinal lymph nodes, presented with multiple, asymptomatic, erythematous papules and nodules prevalent since nine years over the trunk and extremities.
Khopkar, Uday, Misri, Rachita, Dandale, Ameet, Patel, Vidula, Kharkar, Vidya, Mahajan, Sunanda   +5 more
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Possible roles of Epstein-Barr virus in Castleman disease [PDF]

, 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
Chen Chih-Hao, Tzu-Ti Hung, Tsang-Pai Liu, Hung Tzu-Ti, Hung-Chang Liu, Liu Tsang-Pai, Liu Hung-Chang, Chih-Hao Chen   +7 more
core   +2 more sources

Castleman disease of childhood: A case report

, 2001
Giant lymph node hyperplasia (Castleman disease) is uncommon in children and rare in infancy. A 9-month-old girl with a left cervical mass, was followed up for six months.
Filiz Bolat, Derya Alabaz, Melek Ergin, Aysun Uğuz, Gülfiliz Gönlüşen   +4 more
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Primary effusion lymphoma metachronous to multicentric Castleman disease in an immunocompetent patient

, 2020
Human Herpesvirus 8 (HHV8) has been associated with a wide spectrum of B-cell lymphoproliferative disorders, including Primary Effusion Lymphoma, Multicentric Castleman Disease, HHV8-positive Diffuse Large B-cell Lymphoma, not otherwise specified and ...
Zizzo M, Parente P, Zanelli M, Graziano P, Covelli C, Ascani S, Carosi I   +6 more
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Castleman disease: A case with atypical presentation

, 2004
Castleman disease is a benign lymphoproliferative disorder characterized by enlarged lymph nodes. In children the disease is rare, usually localized, and asymptomatic. Resection of the node is almost always curative. A case is reported that was diagnosed
Yildiz, K, Kalyoncu, MUKADDES, Okten, A, Yaris, N, Cakir, M   +4 more
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Study of the morphological patterns and association of Epstein-Barr virus and human herpes virus 8 in acquired immunodeficiency deficiency syndrome-related reactive lymphadenopathy

Indian Journal of Pathology and Microbiology, 2010
Aims: Study of the morphological patterns of acquired immunodeficiency syndrome (AIDS)-related lymphadenopathy. Settings and Design: We retrospectively selected cases of AIDS-related benign lymphadenopathy.
Gujral S, Gandhi J, Valsangkar S, Shet T, Epari S, Subramanian P   +5 more
doaj  

A Rare Case Report of Simultaneous Medullary Thyroid Cancer and Castleman\'s Disease

پزشکی بالینی ابن سینا, 2012
Introduction: Medullary thyroid cancer (MTC) is a neuroendocrine tumor which originates from the parafollicular cells. The prognosis of MTC is poor and thyroidectomy can be effective.
Alireza Rastgoo Haghi, Mohammad Amin Fereiduni, Arash Dehghan, Mohammad Shayani Nasab, Moghadaseh Shams   +4 more
doaj  

Huge splenomegaly, a rare presentation of multicentric Castleman’s disease in an HIV-infected patient: a case report and literature review

HIV & AIDS Review. International Journal of HIV-Related Problems
Introduction Castleman’s disease (CD) is characterized by non-neoplastic lymph node hyperplasia, and may be localized in a single lymph node (unicentric) or occurs systemically (multicentric).
Malihe Hasannezad, Abdolkarim Haji Ghadery, Sara Ghaderkhani, Armin Vazirian, Fereshteh Ameli, Farid Azmoudeh-Ardalan, Mohammad Reza Rafiian Naini, Ladan Abbasian   +7 more
doaj   +1 more source

Enfermedad de Castleman. Reporte de 14 casos de 1990-2002 en el "Hospital Dr. Rafael Angel Calderón Guardia", dos con presentación inusual y revisión de literatura

Acta Médica Costarricense, 2005
La enfermedad de Castleman (hamartoma linfoideo, linfoma gigante benigno, hiperplasia angiofolicular de los nódulos linfáticos) es un transtorno linfoproliferativo raro, de curso usualmente benigno de etiología desconocida y pobremente entendido. Resulta
Eduardo Fiedler-Velásquez, Charles Gourzong- Taylor, Pedro Goyenaga-Hernández, Jairo López-Castro   +3 more
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A patient with WT syndrome and Castleman disease

, 1995
WT syndrome, an autosomal dominant condition, combines hematological abnormalities with mild lib defects. Anemia, pancytopenia, leukemia and lymphoma can occur at varying ages from childhood to middle age.
BALIK E., ÇOKER M., Özkınay F., NIŞLI G., KAVAKLI K., ÖZTOP S., VERGIN C., ÇETINGÜL N., AKAR O., SOYDAN S.   +9 more
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