Literature DB >> 9127317

Primary leiomyosarcomas of the lung: a clinicopathologic and immunohistochemical study of 18 cases.

C A Moran1, S Suster, S L Abbondanzo, M N Koss.   

Abstract

We studied 18 patients with primary malignant smooth muscle tumors of the lung (7 women and 11 men, 5-76 yr old, with a mean age of 50 yr). Lesions varied from 1.7 to 10 cm in greatest diameter. The tumors were classified as low (4 cases), intermediate (2), or high grade (12). Low-grade lesions were characterized by an orderly proliferation of fascicles of spindle cells that intersected at right angles and showed oval-to-spindle cells with cigar-shaped nuclei, minimal pleomorphism, and low mitotic activity, without hemorrhage or necrosis. Intermediate-grade lesions retained the fascicular configuration but showed increased cellularity with atypia and dense chromatin pattern, occasional pleomorphism, and mild increase in mitotic activity. High-grade lesions showed high cellularity, marked pleomorphism and atypia, frequent areas of hemorrhage and necrosis, and high mitotic activity. Immunohistochemical studies in 16 cases showed positive staining of tumor cells with smooth muscle actin in 12, desmin in 5, and coexpression of actin and/or desmin and keratin in 3. Six patients with low- and intermediate-grade lesions were alive and well from 2 to 12 years after diagnosis (mean follow-up time, 6 yr); 8 with high-grade lesions died of their tumors with widespread metastases from 1 to 24 months after diagnosis (median survival time, 5 mo). One patient whose tumor showed features of high-grade leiomyosarcoma was alive and well 12 years after surgery. Three patients with high-grade tumors were lost to follow-up. Our findings suggest that histologic grade may be the most reliable prognostic parameter for predicting clinical behavior in primary leiomyosarcoma of the lung and that smooth muscle actin is the most sensitive immunohistochemical marker for establishing the diagnosis in these tumors. Primary leiomyosarcoma should be considered in the differential diagnosis of pulmonary spindle cell neoplasms; histologic grading may be of value in the planning of therapy and assessment of prognosis for these lesions.

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Year:  1997        PMID: 9127317

Source DB:  PubMed          Journal:  Mod Pathol        ISSN: 0893-3952            Impact factor:   7.842


  4 in total

1.  The immunohistochemical characterization of sarcomatoid malignant mesothelioma of the pleura.

Authors:  Lucian R Chirieac; Geraldine S Pinkus; Jack L Pinkus; John Godleski; David J Sugarbaker; Joseph M Corson
Journal:  Am J Cancer Res       Date:  2010-09-30       Impact factor: 6.166

2.  Risk Assessment of Visceral Sarcomas: A Comparative Study of 2698 Cases from the SEER Database.

Authors:  Nooshin K Dashti; Justin M M Cates
Journal:  Ann Surg Oncol       Date:  2021-02-04       Impact factor: 5.344

3.  Primary Pulmonary Leiomyosarcoma: An Unusual Cause of Pleural Effusion.

Authors:  Syed Hamza Bin Waqar; Biplov Adhikari; Navid Salahi; Sara Ahmed; Sadafsadat Mirkarimi
Journal:  Cureus       Date:  2022-04-04

4.  Surgical treatment for recurrent pulmonary artery sarcoma.

Authors:  Atsushi Omura; Satoshi Tobe; Kazunori Yoshida; Masahiro Yamaguchi
Journal:  Gen Thorac Cardiovasc Surg       Date:  2008-01-22
  4 in total

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