Castleman's Disease
Tumor enucleation for Castleman’s disease in the pulmonary hilum: a case report
... Case presentation: The patient was a 15-year-old male with a tumor in the right pulmonary hilum. Endobronchial ultrasound-guided transbronchial needle aspiration was performed but no specific findings were obtained from ...
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Successful treatment of a Caucasian case of multifocal Castleman’s disease with TAFRO syndrome with a pathophysiology targeted therapy - a case report
... Tissue samplings of inguinal and mediastinal nodules (by bronchoscopy) were not diagnostic. After an initial improvement with high dose steroid therapy (methylpred- nisolone intravenously at 1 mg/kg for two weeks, then ...
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Castleman’s Disease of the Pleura: Case Presentation and Review of Literature
... Castleman’s Disease is a very rare medical disease and the presence of this condition in the pleura is even rarer and there are only few reported ...castleman’s disease instead of solitary lesions ...
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Multicentric Castleman’s disease with voltage-gated potassium channel antibody-positive limbic encephalitis: a case report
... Castleman’s disease (CD) is a rare lymphoproliferative dis- order characterized by enlarged, hyperplastic lymph nodes that can mimic lymphoma. First described in 1954 [1], CD occurs in several histologic variants, ...
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A case report of syndrome of inappropriate antidiuretic hormone secretion with Castleman’s disease and lymphoma
... SIADH is not difficult to diagnose in clinic. It can be secondary to a variety of disorders, such as medications, malignancies, surgery, and HIV infection or be idio- pathic [1,2]. While SCLC is the primary malignancy ...
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Retroperitoneal Castleman’s disease: advocating a multidisciplinary approach for a rare clinical entity
... Angiofollicular lymph node hyperplasia, or Castleman’s disease (CD), is a rare neoplastic disease first identified in 1956 by Castleman and colleagues [1]. It has been de- scribed mainly in case ...
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Castleman’s disease in the retroperitoneal space mimicking a paraspinal schwannoma: a case report
... the disease, a preoperative diagnosis of UCD was not made in previous case reports of UCD [10,11], resulting in the surgical exploration of suspicious malignant tumors, including liposarcomas [12], malignant ...
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Relapses of primary cutaneous anaplastic large-cell lymphoma in a female immunocompetent patient with persistent chlamydophila pneumoniae and human herpesvirus 8 infection
... ’ s sar- coma (KS), Multicentric Castleman’s Disease (MCD), and Primary Effusion Lymphomas (PEL), and associated to other lymphoproliferative disorders occurring primar- ily in immunosuppresed patients [22, ...
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Castleman disease of the hyaline vascular variant transforming to POEMS syndrome as endpoint: a case report
... with Castleman dis- ease without any clinical evidence of POEMS ...ical Castleman disease variant of POEMS syndrome has no clonal PCD and typically little to no peripheral neur- opathy, therefore ...
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Case Report Clinical and radiological features of parapancreatic hyaline-vascular Castleman disease: a case report and literature review
... Castleman’s disease (LCD), only affects a group of lymph nodes, is defined as a single, benign lesion which usually affects young people [8, ...tleman’s disease (MCD) which always affects more than one ...
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Castleman’s disease in the HIV-endemic setting
... Castleman’s disease (CD), first described by Benjamin Castleman in 1954, is a giant or angiofollicular lymph node hyperplasia, described as a rare monotypic polyclonal B-cell lymphoproliferative disorder ...
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Impact of siltuximab on patient-related outcomes in multicentric Castleman’s disease
... Castleman’s disease (MCD) is a rare, widespread lymphoproliferative disorder and a life-threatening disease involving hyperactivity of the immune system, excessive proinflammatory cytokine release, immune ...
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Diagnosis and treatment of CD20 negative B cell lymphomas
... CD20 negative B cell non-Hodgkin lymphoma (NHL) is rare and accounts for approximately 1-2% of B cell lymphomas. CD20- negative NHL is frequently associated with extranodal involvement, atypical morphology, aggressive ...
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The efficacy and safety of anti-interleukin-6 receptor monoclonal blockade in a renal transplant patient with Castleman disease: early post-transplant outcome
... hyperplasia has been implicated in its pathogenesis [1– 3]. The clinical features include generalized lymphaden- opathy, organomegaly, and systemic manifestations, such as fatigue, a low-grade fever, and weight loss. ...
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Case Report Primary Castleman disease in peripancreatic tissue regarded as pancreatic malignance: a case report
... Castleman disease is rare and often ignored in clinical. It still needs to pay more attention when a mass is found in abdomen which may be regarded as the tumor. It is known that surgi- cal removal of the ...
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Iron-Deficiency Anemia in Castleman Disease: Implication of the Interleukin 6/Hepcidin Pathway
... In addition to occasional autoimmune hemolytic anemia, unexplained iron-deficiency anemia has been reported in childhood Castleman dis- ease (CD). The recent discovery of hepcidin has regenerated the re- search on ...
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Severe refractory TAFRO syndrome requiring continuous renal replacement therapy complicated with Trichosporon asahii infection in the lungs and myocardial infarction: an autopsy case report and literature review
... Castleman disease (CD), first described by Castleman et ...the disease was further divided into the following three groups: hyaline vascular (HV) type, plasma cell (PC) type, and mixed type ...
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Case Report Castleman disease variant of POEMS syndrome complicated with multiple cerebral infarction: a rare case report and review of literature
... changes. Castleman disease is a lymphoproliferative disorder that can be present in POEMS patients, which can be defined as Castleman disease variant of POEMS ...
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Case Report Multicentric Castleman disease as a rare cause of nephrotic syndrome: a case report
... The pathogenesis of CD remains poorly under- stood. MCD has been shown to frequently cor- relate with HIV or HHV-8 infection [7]. Those without HHV-8 are called idiopathic Castleman disease, a subset of MCD ...
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Extranodal Castleman Disease of Lower Extremities: A Case Report of a Rare Presentation
... The reported cases suggested that this disease was more prevalent among young individuals. Seven of the eight reported cases aged 15 - 37 years, the remaining one reported by Eward et al., was 76 at the time of ...
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