Angiofollicular lymph node hyperplasia arising from the intercostal space.

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Angiofollicular lymph node hyperplasia arising from the intercostal space.

Angiofollicular lymph node hyperplasia (Castleman's disease) was first described in 1956 by Castleman et al' as asymptomatic large, benign hyperplastic mediastinal lymph nodes that resembled thymoma. This disease has been reported in various sites and organs, but a careful search of published reports showed no case arising from the intercostal space. We report a case that arose in the chest wall.

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Angiofollicular lymph node hyperplasia (Castleman).

Six personally observed cases of this lesion are reported and the literature is reviewed. One hundred and thirty-four cases have been reported to date. The lesion has occurred in many sites, but is commonest in the thorax (60%), abdomen (11%), neck (14%), and axilla (4%). Ninety per cent of cases are symptomless or have only the pressure symptoms, 10% have systemic signs, namely, fever, raised ...

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Angiofollicular lymph node hyperplasia with amyloidosis.

Two cases of angiofollicular lymph node hyperplasia are described, one of the solitary plasma cell type the other of the multicentric hyaline vascular type. Both cases illustrate the wide ranging clinical and pathological findings associated with this condition but both also have unusual features. The solitary plasma cell lesion had an exceptional 32 year clinical history and was associated wit...

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Angiofollicular lymph node hyperplasia with amyloidosis

Two cases of angiofollicular lymph node hyperplasia are described, one of the solitary plasma cell type the other of the multicentric hyaline vascular type. Both cases illustrate the wide ranging clinical and pathological findings associated with this condition but both also have unusual features. The solitary plasma cell lesion had an exceptional 32 year clinical history and was associated wit...

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Intestinal lymphangiectasia associated with angiofollicular lymph node hyperplasia (Castleman's disease).

A patient presenting with predominantly gastrointestinal symptoms and a history of myocardial infarction was found to have ascites, hepatosplenomegaly, para-aortic lymphadenopathy, thrombocytosis, and a paraproteinaemia. A jejunal biopsy specimen showed lymphangiectasia and histology of the spleen and lymph nodes showed angiofollicular hyperplasia or Castleman's disease of the hyaline vascular ...

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ژورنال

عنوان ژورنال: Thorax

سال: 1988

ISSN: 0040-6376

DOI: 10.1136/thx.43.4.337