Neuro-ophthalmological findings in TAFRO syndrome in a patient from South America, a variant of multicentric Castleman's disease.

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Neuro-ophthalmological findings in TAFRO syndrome in a patient from South America, a variant of multicentric Castleman's disease.

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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2017年学术文章

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2017年学术文章

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Neuro-ophthalmological finding ...... ticentric Castleman's disease.

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Neuro-ophthalmological finding ...... ticentric Castleman's disease.

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Item

label

Neuro-ophthalmological finding ...... ticentric Castleman's disease.

@en

Neuro-ophthalmological finding ...... ticentric Castleman's disease.

@nl

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Neuro-ophthalmological finding ...... ticentric Castleman's disease.

@en

Neuro-ophthalmological finding ...... ticentric Castleman's disease.

@nl

P1476

Neuro-ophthalmological finding ...... ticentric Castleman's disease.

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P2093

Alvaro Ortiz

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Gabriel Frederick

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Harold Rodríguez

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Jacobo Ortiz

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Marcela Peralta

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Pedro Cárdenas

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P2860

Japanese variant of multicentric castleman's disease associated with serositis and thrombocytopenia--a report of two cases: is TAFRO syndrome (Castleman- Kojima disease) a distinct clinicopathological entity?

Successful treatment of a Caucasian case of multifocal Castleman's disease with TAFRO syndrome with a pathophysiology targeted therapy - a case report.

TAFRO syndrome: 2 cases and review of the literature.

Clinicopathologic analysis of TAFRO syndrome demonstrates a distinct subtype of HHV-8-negative multicentric Castleman disease.

TAFRO syndrome successfully treated with tocilizumab: A case report and systematic review.

Proposed diagnostic criteria, disease severity classification and treatment strategy for TAFRO syndrome, 2015 version.

Aggressive TAFRO syndrome with reversible cardiomyopathy successfully treated with combination chemotherapy.

A case of TAFRO syndrome, a variant of multicentric Castleman's disease, successfully treated with corticosteroid and cyclosporine A.

Localized mediastinal lymphnode hyperplasia resembling thymoma.

Polyneuropathy, organomegaly, endocrinopathy, M-protein and skin changes (POEMS syndrome): a paraneoplastic syndrome.

P2888

s10792-017-0636-x

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scholarly article

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10.1007/S10792-017-0636-X

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P577

2017-07-27T00:00:00Z

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P698

28752346

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