'Pseudomesotheliomatous' carcinomas of the pleura: a 10-year analysis of cases from the Environmental Lung Disease Research Group, Cardiff

被引:60
作者
Attanoos, RL
Gibbs, AR
机构
[1] Llandough Hosp, Dept Histopathol, Cardiff, S Glam, Wales
[2] Vale NHS Trust, Dept Histopathol, Cardiff, S Glam, Wales
关键词
mesothelioma; pleurotropic neoplasms;
D O I
10.1046/j.1365-2559.2003.01674.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Aims: To undertake a clinicopathological study of diffuse serosal neoplasms of epithelial histogenesis which clinically and pathologically mimic malignant pleural mesothelioma. Methods and results: Over a 10-year (1990-2000) study period 53 carcinomas mimicking diffuse pleural mesothelioma ('pseudomesotheliomatous' carcinoma) were identified. The study group comprised 50 men and three females, age range 33-77 (median 68) years. In 46 (87%) cases there was a history of smoking and in 40 (76%) cases a history of asbestos exposure. Histologically the pleural 'pseudomesotheliomatous' carcinomas could be divided into two broad groups: primary pulmonary carcinomas with florid pleurotropic growth (n = 47), of which 34 (70%) were adenocarcinomas; and diffuse carcinomatous involvement of the pleura by metastatic tumour (n = 6). This latter group comprised two transitional cell carcinomas of bladder, one renal (clear) cell carcinoma, one ductal pancreatic adenocarcinoma, one prostatic adenocarcinoma and one squamous cell carcinoma of parotid gland origin. Follow-up data were available in 35 cases. Regardless of tumour type, survival was poor (median 8 months) and comparable to diffuse pleural mesothelioma. Conclusions: Pleural 'pseudomesotheliomatous' carcinomas are uncommon (comprising 6% of referrals), pathologically heterogeneous tumours with poor prognosis. Tissue diagnosis should be obtained in all cases of suspected diffuse pleural neoplasia. By light microscopy and immunophenotype many of the tumours mimicked malignant mesothelioma. In particular, an awareness that all neoplasms exhibiting squamous differentiation may express cytokeratin 5/6 and thrombomodulin is important to prevent misinterpretation. In this respect, calretinin is regarded as the most specific and sensitive mesothelial marker. Misdiagnosis may have medico-legal implications in asbestos-related compensation claims.
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收藏
页码:444 / 452
页数:9
相关论文
共 43 条
[1]   A COMPARATIVE IMMUNOHISTOCHEMICAL STUDY OF MALIGNANT MESOTHELIOMA AND RENAL-CELL CARCINOMA - THE DIAGNOSTIC UTILITY OF LEU-M1, BER EP4, TAMM-HORSFALL PROTEIN AND THROMBOMODULIN [J].
ATTANOOS, RL ;
GODDARD, H ;
THOMAS, ND ;
JASANI, B ;
GIBBS, AR .
HISTOPATHOLOGY, 1995, 27 (04) :361-366
[2]   Primary thymic epithelial tumours of the pleura mimicking malignant mesothelioma [J].
Attanoos, RL ;
Galateau-Salle, F ;
Gibbs, AR ;
Muller, S ;
Ghandour, F ;
Dojcinov, SD .
HISTOPATHOLOGY, 2002, 41 (01) :42-49
[3]   Mesothelioma-binding antibodies: Thrombomodulin, OV 632 and HBME-1 and their use in the diagnosis of malignant mesothelioma [J].
Attanoos, RL ;
Goddard, H ;
Gibbs, AR .
HISTOPATHOLOGY, 1996, 29 (03) :209-215
[4]   Malignant vascular tumours of the pleura in "asbestos" workers and endothelial differentiation in malignant mesothelioma [J].
Attanoos, RL ;
Suvarna, SK ;
Rhead, E ;
Stephens, M ;
Locke, TJ ;
Sheppard, MN ;
Pooley, FD ;
Gibbs, AR .
THORAX, 2000, 55 (10) :860-863
[5]  
ATTANOOS RL, 1996, HISTOPATHOLOGY, V29, P241
[6]  
Attanoos RL, 2001, EUR RESPIR J, V18, p534S
[7]  
BATTIFORA H, 1995, ATLAS TUMOUR PATHOL, P37
[8]   MULTIPLE-MARKER IMMUNOHISTOCHEMICAL PHENOTYPES DISTINGUISHING MALIGNANT PLEURAL MESOTHELIOMA FROM PULMONARY ADENOCARCINOMA [J].
BROWN, RW ;
CLARK, GM ;
TANDON, AK ;
ALLRED, DC .
HUMAN PATHOLOGY, 1993, 24 (04) :347-354
[9]   CARCINOMATOUS INVOLVEMENT OF PLEURA - ANALYSIS OF 96 PATIENTS [J].
CHERNOW, B ;
SAHN, SA .
AMERICAN JOURNAL OF MEDICINE, 1977, 63 (05) :695-702
[10]   Keratin expression in human tissues and neoplasms [J].
Chu, PG ;
Weiss, LM .
HISTOPATHOLOGY, 2002, 40 (05) :403-439