Abstract
A case of pulmonary hyalinizing granuloma (PHG) with Castleman's disease in a 43-year-old man is presented. He was asymptomatic, but the disease was recognized due to a routine chest roentgenographic study. Anemia, multiple lymphadenopathy, hypoalbuminemia and polyclonal hypergamma-globulinemia were observed. Histological examination of cervical lymph nodes revealed the plasma cell type of Castleman's disease. The diagnosis of PHG was confirmed by videoassisted thoracoscopical lung biopsy, and the immuno-histochemical staining of lamellar fibrosis for types I and III collagen was positive. (Internal Medicine 33: 689-691, 1994). © 1994, The Japanese Society of Internal Medicine. All rights reserved.
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Atagi, S., Sakatani, M., Akira, M., Yamamoto, S., & Ueda, E. (1994). Pulmonary Hyalinizing Granuloma with Castleman’s Disease. Internal Medicine, 33(11), 689–691. https://doi.org/10.2169/internalmedicine.33.689
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