4.5 Article

Primary Giant Cell Tumors of the Lung A Clinicopathologic and Immunohistochemical Study of 3 Cases

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AMERICAN JOURNAL OF SURGICAL PATHOLOGY
卷 45, 期 8, 页码 1151-1154

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LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/PAS.0000000000001686

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giant cells; lung; immunohistochemistry; sarcoma; carcinoma

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This article presents three cases of primary giant cell tumors of the lung in male patients aged between 43 and 54 years, who presented with nonspecific symptoms. After surgery, two patients were followed up for 12 months without evidence of recurrence or metastasis. These cases represent an unusual occurrence that should be considered in the differential diagnosis of primary pulmonary tumors rich in multinucleated giant cells.
Three cases of primary giant cell tumors of the lung akin to those described in the soft tissues are presented. The patients are 3 men between the ages of 43 and 54 years who presented with nonspecific symptoms of cough, chest pain, and shortness of breath. None of the patients had any prior history of malignancy anywhere else. Diagnostic imaging disclosed the presence of an intrapulmonary mass. All the patients underwent lobectomy. Grossly, the tumors were described as solid, slightly hemorrhagic, and measuring between 1.8 and 2.4 cm in greatest diameter. Histologically, the tumors were characterized by a dual population of multinucleated giant cells admixed with a mononuclear proliferation. Nuclear atypia was mild to moderate, and mitotic activity varied but was under 5 mitotic figures per 10 high power fields. Immunohistochemical stains showed positive staining for vimentin, CD68, and cathepsin K, whereas the tumors were negative for keratin, TTF-1, p40, S-100 protein, and SABT-2. Clinical follow-up was obtained in 2 patients who have remained alive and without evidence of recurrence or metastasis up to 12 months after surgery. One patient was lost to follow-up. The current neoplasms represent a tumor that to the best of our knowledge has not been reported as a primary neoplasm of the lung. The cases herein described represent an unusual occurrence and should be maintained in the differential diagnosis of primary pulmonary tumors rich in multinucleated giant cells.

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