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PATHOLOGY
Spindle
Cell Lesions of the Adult Prostate
Hansel DE, Herawi M, Montgomery E, Epstein JI
Department of Pathology, The Johns Hopkins Hospital, Baltimore, MD, USA
Mod Pathol. 2007; 20: 148-58
- Prostatic
spindle cell lesions are diagnostically challenging and encompass a
broad array of benign and malignant processes. A subset of these lesions
arises only within the prostate and generally represents entities that
originate from the prostate epithelium or stroma, such as sclerosing
adenosis, sarcomatoid carcinoma, stromal tumors of uncertain malignant
potential (STUMP), and stromal sarcoma. Another subset of spindle cell
tumors that involve the prostate are also found at other sites and include
solitary fibrous tumor, leiomyosarcoma, and neural lesions among others.
Finally, tumors may secondarily involve the prostate yet present as
primary prostatic processes, as is evident with several cases of gastrointestinal
stromal tumors (GIST). The utility of ancillary studies, including immunohistochemistry,
is often limited and the main criteria for diagnosis are the morphologic
findings by routine H&E stain. This review addresses the various
entities that may present as spindle cell tumors within the adult prostate
and discusses the functional aspects of the differential diagnosis of
these lesions.
- Editorial
Comment
Spindle cell lesions are rare in the prostate. Among these lesions is
worth commenting for the urologists sarcomatoid carcinoma and the lesions
proposed by the authors to be called STUMP. There is a lot of debate
in the literature about the terms sarcomatoid carcinoma vs. carcinosarcoma.
These terms apply to tumors that show spindling of the cells sometimes
with heterologous differentiation like osteosarcoma, condrosarcoma,
angiosarcoma and others. There is a tendency to call these cases sarcomatoid
carcinoma with heterologous differentiation based on studies that show
a monoclonal origin for these tumors.
Stromal tumors of uncertain malignant potential (called by the authors
STUMP) encompass a group of lesions that most of the times are hard
to establish histologically the biological behavior in contrast to frankly
sarcomatous lesions like leiomiosarcoma, rabdomiosarcoma and others.
STUMP includes several patterns of lesions originating from the specialized
stroma of the prostate: phyllodes tumor of the prostate, hypercellular
stroma with scattered atypical yet degenerative cells, and extensive
overgrowth of hypercellular stroma with the histology of a stromal nodule
(1). STUMPS are considered neoplastic, based on the observations that
they may diffusely infiltrate the prostate gland and extent into adjacent
tissues, and often recur. Although most cases of STUMP do not behave
in an aggressive fashion, occasional cases have been documented to recur
rapidly after resection and a minority has progressed to stroma sarcoma.
Reference
1. Cheville J, Algaba F, Boccon-Gibod L, Billis A, Cheng L, Epstein JI,
Furusato M, Lopez-Beltran A: Mesenchymal Tumours. In: Eble JN, Sauter
G, Epstein JI, Sesterhenn (eds.), Pathology & Genetics, Tumours of
the Urinary System and Male Genital Organs. World Health Organization
Classification of Tumours, IARC Press, Lyon, 2004.
Dr.
Athanase Billis
Full-Professor of Pathology
State University of Campinas, Unicamp
Campinas, Sao Paulo, Brazil |