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1.
Nihon Kokyuki Gakkai Zasshi ; 48(7): 497-501, 2010 Jul.
Article in Japanese | MEDLINE | ID: mdl-20684212

ABSTRACT

A 72-year-old man complained of dyspnea and epigastric pain. He was admitted to our hospital with progressive dyspnea and abnormal chest radiograph findings. Chest CT scan on admission showed multiple nodular shadows with and without air-bronchograms, vessels or cavitation. Transbronchial and percutaneous lung biopsy specimens demonstrated poorly differentiated carcinoma. Pulmonary metastases were suspected, but their primary origin was unknown. Chest and abdominal CT scans on the 18th hospital day showed a giant tumor of the small intestine and rapid progression of the pulmonary tumor, forming cavitation. The patient's condition worsened, and he died on the 51st hospital day. At autopsy, a final diagnosis of T-cell lymphoma of the small intestine and pulmonary metastases was obtained. This is a rare case which was found primarily based on the characteristic radiologic features of pulmonary metastases.


Subject(s)
Intestinal Neoplasms/diagnosis , Intestine, Small , Lung Neoplasms/secondary , Lymphoma, T-Cell/diagnosis , Aged , Humans , Intestinal Neoplasms/pathology , Lung Neoplasms/diagnostic imaging , Lymphoma, T-Cell/pathology , Male , Radiography
2.
Nihon Kokyuki Gakkai Zasshi ; 47(8): 711-6, 2009 Aug.
Article in Japanese | MEDLINE | ID: mdl-19764514

ABSTRACT

We report a rare case of bilateral hearing loss and diffuse alveolar hemorrhage associated with microscopic polyangitis (MPA). A 75-year-old woman complained of hearing loss. Two months later, she was admitted due to rapidly progressing dyspnea. Chest radiography and CT scan showed diffuse bilateral consolidations. Mechanical ventilation was required for respiratory insufficiency. Laboratory data demonstrated anemia and renal failure. Steroid pulse therapy and antibiotics were initiated. On day 2, bronchoalveolar lavage showed fresh blood-like fluid, which suggested diffuse alveolar hemorrhage (DAH). Serum level of myeloperoxidase-antineutrophil cytoplasmic antibody (MPO-ANCA) was elevated. Therefore, DAH and rapidly progressive glomerulonephritis associated with MPA were diagnosed. Treatment was also performed with cyclophosphamide pulse therapy and plasmapheresis. Her pulmonary lesion improved dramatically. We emphasize the effectiveness of bronchoalveolar lavage for prompt and accurate diagnoses. Moreover, this case report also suggests that early cyclophosphamide therapy and plasmapheresis may be an effective treatment for MPA with diffuse alveolar hemorrhage. In contrast, hearing loss did not improve after therapy. Some cases reported hearing loss as a rare symptom of MPA. We also suspect that hearing loss may be a complication of MPA. We reported this case because there has been no description of hearing loss accompanying DAH associated with MPA.


Subject(s)
Hearing Loss, Bilateral/etiology , Hemorrhage/etiology , Lung Diseases/etiology , Microscopic Polyangiitis/complications , Pulmonary Alveoli , Aged , Bronchoalveolar Lavage , Female , Humans , Lung Diseases/therapy
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