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RadioGraphics, 2023
Castleman disease (CD) is a group of rare and complex lymphoproliferative disorders that can manifest in two general forms: unicentric CD (UCD) and multicentric CD (MCD). These two forms differ in clinical manifestation, imaging appearances, treatment options, and prognosis.
Marika A. Pitot +9 more
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Castleman disease (CD) is a group of rare and complex lymphoproliferative disorders that can manifest in two general forms: unicentric CD (UCD) and multicentric CD (MCD). These two forms differ in clinical manifestation, imaging appearances, treatment options, and prognosis.
Marika A. Pitot +9 more
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Castleman Disease Pathogenesis
Hematology/Oncology Clinics of North America, 2018Castleman disease (CD) describes a group of heterogeneous disorders with common lymph node histopathologic features, including atrophic or hyperplastic germinal centers, prominent follicular dendritic cells, hypervascularization, polyclonal lymphoproliferation, and/or polytypic plasmacytosis.
David C, Fajgenbaum, Dustin, Shilling
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Treatment of castleman’s disease
Current Treatment Options in Oncology, 2005Castleman's disease (CD) was first described in 1954 and further defined in 1956 by Castleman. Since then much has been learned about the heterogeneity of this condition. Subsequently, three pathologic classifications have been developed (hyaline vascular variant, plasma cell variant, and mixed variant) and two clinical classifications (unicentric ...
Angela, Dispenzieri, Morie A, Gertz
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Retroperitoneal Castleman's Disease
Urology, 2010A 56-year-old postmenopausal woman with a history of colon cancer status after left hemicolectomy presented to our institution with abdominal pain, early satiety, and weight loss. Computerized tomography scan showed a large, enhancing, fat-containing mass displacing the left kidney posteriolaterally suspicious for a retroperitoneal liposarcoma.
A Ari, Hakimi +3 more
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Castleman's disease in children
Journal of Pediatric Surgery, 1986A three and one-half-year-old girl and a 12-year-old boy presented with features of the two clinical presentations of Castleman's disease or giant lymph node hyperplasia. The girl presented with anemia, fever, night sweats, hypergammaglobulinemia, and a palpable abdominal mass.
R W, Powell +3 more
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Journal of Computer Assisted Tomography, 1983
Computed tomography in a case of mesenteric Castleman tumor showed a well-circumscribed homogeneous soft tissue density mass with moderate contrast enhancement after injection of contrast material. These findings correlate well with previously reported mediastinal Castleman tumors.
E, Iida +5 more
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Computed tomography in a case of mesenteric Castleman tumor showed a well-circumscribed homogeneous soft tissue density mass with moderate contrast enhancement after injection of contrast material. These findings correlate well with previously reported mediastinal Castleman tumors.
E, Iida +5 more
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Castleman's disease of the urachus
Urology, 2004Castleman's disease (angiofollicular lymphoid hyperplasia) is a rare heterogeneous group of lymphoproliferative disorders of uncertain cause. Most cases occur as mediastinal masses, although extrathoracic involvement has been reported. Castleman's disease involving the genitourinary tract, one of the most infrequent organ systems affected, has so far ...
Udo, Rudloff +4 more
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Castleman’s disease of the spleen
Acta Chirurgica Belgica, 2016Castleman's disease (CD), also known as giant or angiofolicular lymphoid hyperplasia or lymphoid hamartoma, is a group of atypical lymphoproliferative disorders that share common lymph node histological features and may be localized either to a single lymph node (unicentric) or occur systemically (multicentric).Herein, we present a rare case of a of 75-
Dimitrios, Mantas +4 more
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Castleman’s disease of the pleura
General Thoracic and Cardiovascular Surgery, 2011Castleman's disease is a rare benign disease of the lymph nodes. Its origin from the pleura is rare. Surgical excision, when feasible, appears to provide good results. We encountered a patient who had the disease arising from the parietal pleura. We present the clinical scenario, investigations, and our management of the patient.
Rajaram, Burrah +6 more
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Retroperitoneal Castleman Lymphoma
Beiträge zur Pathologie, 1973Summary A tangerine-sized, retroperitoneal tumor in the region of the right adnexe, clinically suspicious of an ovarian or renal tumor, was histologically identified as an angiomatous Castleman lymphoma with distinct splenization. The considerable morphological variance of Castleman's lymphoma ranging from “thymization” (better “hasallization”) to ...
K O, Schmid +4 more
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