Predicting Clinical Outcome for Uterine Smooth Muscle Neoplasms with a Reasonable Degree of Certainty

1997 ◽  
Vol 4 (2) ◽  
pp. 95-104 ◽  
Author(s):  
Teri A. Longacre ◽  
Michael R. Hendrickson ◽  
Richard L. Kempson
2000 ◽  
Vol 124 (2) ◽  
pp. 221-227 ◽  
Author(s):  
Lester J. Layfield ◽  
Katharine Liu ◽  
Richard Dodge ◽  
Sanford H. Barsky

Abstract Context.—Accurate categorization of uterine smooth muscle neoplasms by light microscopic examination is difficult. Multiple classification schemes have been proposed based on mitotic rate, nuclear atypia, and the presence or absence of necrosis. None of these classification systems has been entirely successful. Multiple ancillary techniques have been tested for their ability to predict behavior of uterine smooth muscle tumors. Objective.—We assayed 45 smooth muscle neoplasms for a variety of proliferation markers, oncogene protein products, and DNA ploidy level to determine if these markers supplied prognostically useful information over and above that obtained by routine light microscopic assessment. Study Design.—Forty-five uterine smooth muscle neoplasms were assessed for DNA ploidy; silver-staining nucleolar organizer regions (AgNORs); percent nuclear proliferating cell nuclear antigen (PCNA); expression of p53, Her-2/neu, and MDM-2 protein; mitotic rate; and nuclear grade. These markers were correlated with histologic diagnosis and the occurrence of a clinically adverse event (death, metastasis, or recurrence). Results.—Diagnostic category (P < .001), nuclear grade (P < .002), mitotic activity (P < .001), mean AgNORs (P < .001), percent nuclear PCNA (P = .02), and expression of p53 (P = .02) all correlated with clinical outcome. No statistically significant correlation between clinical outcome and the categories MDM-2 expression, Her-2/neu expression, or DNA ploidy was seen. Nuclear grade, p53 expression, mitotic rate, AgNORs, and percent nuclear PCNA correlated with diagnosis. Conclusions.—Diagnostic category, mitotic rate, AgNOR counts, PCNA, and p53 expression dichotomized uterine smooth muscle neoplasms into prognostically favorable and unfavorable groups. Although highly significant, the category AgNORs was no more successful than mitotic rate in dividing uterine smooth muscle neoplasms into prognostically favorable and unfavorable groups. Expression of p53 and percent nuclear PCNA dichotomized uterine smooth muscle neoplasms into prognostic groups, but neither technique reached the level of significance achieved by mitotic rate. Our data indicate that mitotic rate and the classification system of Kempson and Bari are at least as effective as the tested markers in separating uterine smooth muscle neoplasms into prognostic categories.


2020 ◽  
Vol 154 (2) ◽  
pp. 208-214
Author(s):  
Michael J Hwang ◽  
Ashish M Kamat ◽  
Colin P Dinney ◽  
Bogdan Czerniak ◽  
Charles C Guo

Abstract Objectives Bladder cancers invading the muscularis mucosae (MM) are treated differently from those invading the muscularis propria (MP). However, it may be difficult to determine the type of smooth muscle in transurethral resection (TUR) or biopsy specimens. We aimed to investigate the clinicopathologic features of bladder cancers involving smooth muscle of indeterminate type (SMIT) in TUR specimens in comparison with those invading the MM. Methods We identified 103 patients with bladder cancer involving SMIT (n = 27) or the MM (n = 76) in TUR specimens. All patients underwent subsequent restaging TUR or cystectomy. Results Bladder cancer with SMIT invasion showed a significantly higher rate of MP invasion in the subsequent specimens than those invading the MM (52% vs 29%). Lack of MP in the TUR specimens had a significantly higher risk of MP invasion in the subsequent specimens than those with the MP (61% vs 40%). The overall survival time for patients with SMIT invasion was significantly shorter than those with MM invasion. Conclusions Bladder cancers with SMIT invasion in TUR specimens show more frequent cancer upstaging in the subsequent specimens and a poorer clinical outcome than those invading the MM, which highlights the importance of a cancer restaging procedure for these patients.


2021 ◽  
pp. 106689692199779
Author(s):  
Murat Celik

Leiomyoma is a benign mesenchymal tumor that develops from smooth muscle cells. It can present in various histological variants. Leiomyoma with bizarre nuclei is an infrequent variant of uterine smooth muscle neoplasm. It is characterized by focally or diffusely distributed bizarre cells on the background of a typical leiomyoma. These bizarre cells are large, multinucleated, or multilobulated and have an eosinophilic cytoplasm. Even though leiomyomas with bizarre nuclei display benign clinical behavior, their differential diagnosis from leiomyosarcoma can sometimes be difficult. Leiomyoma has been described most commonly in the uterus. There is no case of leiomyoma originating from paratubal cysts described in the literature. In this article, we present a rare case of leiomyoma with bizarre nuclei originating from a paratubal cyst.


1981 ◽  
Vol 256 (11) ◽  
pp. 5436-5442
Author(s):  
J.F. Krall ◽  
S.C. Leshon ◽  
M. Frolich ◽  
S.G. Korenman

1995 ◽  
Vol 27 (5) ◽  
pp. 407-414 ◽  
Author(s):  
B. STIEMER ◽  
R. GRAF ◽  
H. NEUDECK ◽  
R. HILDEBRANDT ◽  
H. HOPP ◽  
...  

1985 ◽  
Vol 126 (1) ◽  
pp. 544-550 ◽  
Author(s):  
Akimitsu Tsutou ◽  
Shun-ichi Nakamura ◽  
Akira Negami ◽  
Keiko Mizuta ◽  
Eikichi Hashimoto ◽  
...  

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