Volume 68, Issue 4 pp. 533-540
Original Article

Pleomorphic giant cell carcinoma of the urinary bladder: an extreme form of tumour de-differentiation

Hemamali Samaratunga

Corresponding Author

Hemamali Samaratunga

Aquesta Pathology, Brisbane, Qld, Australia

University of Queensland, Brisbane, Qld, Australia

Address for correspondence: Professor H Samaratunga, Aquesta Pathology, 21 Lissner Street, Toowong, Brisbane, Qld Q4066, Australia. e-mail: [email protected]Search for more papers by this author
Brett Delahunt

Brett Delahunt

Aquesta Pathology, Brisbane, Qld, Australia

Department of Pathology and Molecular Medicine, Wellington School of Medicine and Health Sciences, Wellington, New Zealand

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Lars Egevad

Lars Egevad

Department of Oncology-Pathology, Karolinska Institute, Stockholm, Sweden

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Michael Adamson

Michael Adamson

Aquesta Pathology, Brisbane, Qld, Australia

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David Hussey

David Hussey

Brisbane Private Hospital, Brisbane, Qld, Australia

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Greg Malone

Greg Malone

Greenslopes Hospital, Brisbane, Qld, Australia

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Kirsten Hoyle

Kirsten Hoyle

Sunshine Coast Private Hospital, Buderim, Qld, Australia

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Tim Nathan

Tim Nathan

Sunshine Coast University Private Hospital, Birtinya, Qld, Australia

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David Kerle

David Kerle

St Vincent's Private Hospital, Lismore, NSW, Australia

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Peter Ferguson

Peter Ferguson

Department of Pathology and Molecular Medicine, Wellington School of Medicine and Health Sciences, Wellington, New Zealand

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John N Nacey

John N Nacey

Department of Surgery and Anaesthesia, Wellington School of Medicine and Health Sciences, Wellington, New Zealand

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First published: 25 July 2015
Citations: 37

Abstract

Aims

Vesical pleomorphic giant cell carcinoma (PGCC) is a variant of urothelial carcinoma (UC) characterized by highly pleomorphic tumour with giant cells. Fewer than 10 cases have been reported, and our aim was to determine the clinical and pathological features of a series of tumours from a specialized uropathology laboratory.

Methods and results

Thirteen cases of PGCC of the bladder were identified. There were nine males and four females, ranging in age from 53 to 92 years (mean 72 years). Associated conventional high-grade UC was seen in eight cases, while three cases also had micropapillary UC and one plasmacytoid UC. UC in situ (CIS) was present in five cases and occasional bizarre cells were seen in both UC and CIS. The proportion of PGCC present varied from 40% to 100% of tumour. Immunostaining performed on 10 cases showed uniform positivity for CK 8/18 and AE1/AE3, while most tumours were positive for CK7, CK20, uroplakin III and GATA binding protein 3 (GATA3). β-human chorionic gonadotrophin (β-hCG) was negative. Of 10 patients with follow-up, five died within 1 year and four are alive with tumour.

Conclusions

The association of PGCC with UC and an overlap in immunoexpression suggests that PGCC represents an extreme form of UC de-differentiation.

The full text of this article hosted at iucr.org is unavailable due to technical difficulties.