A Case of Pulmonary Langerhans' Cell Histiocytosis
Kimiko Sakai1) Yuji Ohtsuki2) Yutaka Hirasawa1) Akihide Hashimoto1) Kenji Nakamura3)
1)Department of Respiratory Medicine, Kita-ishikai Uchiyama Hospital. 275-1, Shiromawari, Uchiko-cho, Kita-gun, Ehime, 791-3310, Japan, 2)Department of Pathology, Kochi Medical School, Kochi, 783-8505, 3)Department of Respiratory Surgery, Ehime National Hospital, Ehime, 791-0281
A 42-yr-old woman was referred to our hospital because of multiple small nodules in a chest radiograph. She had no symptoms such as dyspnea, cough or sputum. A chest CT revealed many centrilobular small nodules and thin-walled cysts with predominance in the peripheral area of the lungs. The specimens obtained by thoracoscopic surgery showed granulomas with scattered eosinophils and numerous Langerhans' cells. The Langerhans' cells were positive for both S-100 protein and CD1a. These findings are compatible with pulmonary Langerhans' cell histiocytosis (LCH). Since the granulomas showed no fibrotic changes, the LCH may have been in its early stages. However, there were clusters of lymphocytes and macrophages around the terminal and respiratory bronchioles, and cystic lesions without cellular infiltrates, in the specimens. The former histologic findings suggested respiratory bronchiolitis causing interstitial lung disease and the latter are indistinguishable from centrilobular emphysema. Therefore, these smoking-related diseases may have been superimposed on the LCH in this patient.
Langerhans cell histiocytosis Eosinophilic granuloma Smoking Pulmonary emphysema Respiratory bronchiolitis-interstitial lung disease
Received 平成14年11月15日
JJRS, 41(9): 685-690, 2003