Uterine epithelioid leiomyosarcoma with c-kit expression and YWHAE gene rearrangement: a case report of a diagnostic pitfall of uterine sarcoma
© The Author(s). 2017
Received: 4 January 2017
Accepted: 27 February 2017
Published: 14 March 2017
Uterine sarcoma is a rare tumor that is often difficult to classify based on morphological and immunohistochemical analysis alone. Limited access to molecular biological analysis in routine practice would hinder making a definitive diagnosis.
In this report, we describe a case of a mesenchymal tumor arising from the uterine cervix in a 52-year-old woman. From microscopic morphology of the resected specimen, epithelioid leiomyosarcoma, high-grade endometrial stromal sarcoma, or uterine gastrointestinal stromal tumor (GIST) were considered as differential diagnoses. The immunophenotype of the tumor featured smooth muscle differentiation and hormone receptor expression. The cell membrane and cytoplasm were positive for c-kit, although no mutation was found in the c-kit or PDGFRA gene. Fluorescence in situ hybridization (FISH) analysis revealed a relatively low frequency of YWHAE rearrangement, whereas there were few NUTM2A and NUTM2B split signals.
In this case, the tumor was not typical of any three of the differential diagnoses mentioned above. However, insufficient frequency of YWHAE, NUTM2A, and NUTM2B gene rearrangement and absence of mutation in both the c-kit and PDGFRA genes suggested that this tumor should be categorized as epithelioid leiomyosarcoma. This is an instructive case showing a potential diagnostic pitfall of uterine sarcoma. Comprehensive approaches including molecular biological techniques are required for definitive diagnosis.
KeywordsYWHAE rearrangement FISH Uterine leiomyosarcoma c-kit
Uterine sarcoma is a rare tumor for which diagnosis is often difficult. According to the 2014 WHO classification, uterine sarcoma consists of leiomyosarcoma, low- and high-grade endometrial stromal sarcoma (ESS), and undifferentiated sarcoma . Uterine gastrointestinal stromal tumor (GIST), although not listed in the WHO classification, is reported in some studies . As newly identified gene rearrangements or immunophenotypes in uterine sarcomas may establish novel disease entities, detailed pathological investigation in each case is becoming increasingly important for appropriate evaluation of the tumor.
We encountered an unusual case of mesenchymal tumor with epithelioid morphology. The tumor arose from the uterine cervix exhibiting relatively low-frequency mitosis, smooth muscle differentiation, and c-kit expression. Furthermore, YWHAE gene rearrangement was detected by fluorescence in situ hybridization (FISH) in the tumor. These findings were suggestive of epithelioid leiomyosarcoma, high-grade ESS, or uterine GIST as differential diagnosis.
Histologically, the cervical mass was below the squamous epithelium and consisted of a nest-like proliferation of less cohesive, epithelioid tumor cells that had rounded nuclei and eosinophilic cytoplasm. The tumor cells had no marked nuclear pleomorphism and prominent nucleoli, and a coarse chromatin pattern was found in the nucleus. Mitotic figures were moderately frequent (4 per high-power field) but atypical mitoses were not present (Fig. 2c). The tumor showed a confluent growth pattern and individual nests of tumor cells were compartmentalized by intricate vasculature (Fig. 2b). There was no apparent involvement of myometrial smooth muscle cells. Foci of extensive necrosis and hemorrhage were found in some areas. A low-grade ESS component, showing uniform cells with round to spindle-shaped nuclei, which were whorled around arteriole-type vessels, was not coexistent in the lesion.
FISH was performed for further molecular biological observations. To detect YWHAE rearrangement derived from chromosomal translocation of t(10;17)(q22;p13)—we used a custom dual-color, split-signal YWHAE probe set for the YWHAE locus on chromosome 17p13 (Chromosome Science Lab, Inc., Sapporo, Japan). The probe set consisted of a 333-kilobase (kb) sequence labeled with SpectrumGreen (telomeric [RP11-143 L7 and RP11-22G12]) and a 303-kb sequence labeled with SpectrumOrange (centromeric [RP11-100 F18 and RP11-60C18]). Rearrangements in the NUTM2A and NUTM2B genes at 10q23 and 10q22, respectively, were characterized using a custom break-apart probe design. The probes were synthesized using oligo-based SureFISH technology (Agilent Technologies, Santa Clara, CA) and labeled with FITC (5’ probe) and Cy3 (3′ probe) fluorophores. The analysis was performed with formalin-fixed, paraffin-embedded specimens sectioned into 3-μm-thick slices, as described previously . The split-signal rate of YWHAE, NUTM2A and NUTM2B was 18%, (Fig. 3d), 0 and 4%, respectively, when 50 nuclei were counted. In contrast, a JAZF1 split, which is a major gene translocation in low-grade ESS,  was not detected.
To investigate KIT and PDGFRA gene mutations, direct sequence analysis was performed. Exons 9, 11, and 13 of the KIT gene and exon 18 of the PDGFRA gene were amplified by polymerase chain reaction using the primers KITexon9F: GGC TTT TGT TTT CTT CCC TTT A, KITexon9R: ATG GTA GAC AGA GCC TAA ACA, KITexon11F: GAT CTA TTT TTC CCT TTC TCC C, KITexon11R: AGC CCC TGT TTC ATA CTG AC, KITexon13F: GCT TGA CAT CAG TTT GCC AG, KITexon13R: GCA GCT TGG ACA CGG CTT T, PDGFRAexon18F: CAG ATG GCT TGA TCC TGA GT, and PDGFRAexon18R: GAG GAT GAG CCT GTC CAG T. The amplified products were purified and sequenced. The sequences of KIT exons 9, 11, and 13 were wild type. In PDGFRA exon 18, substitution of nucleotide C to T, known as a single-nucleotide variant (rs2228230) was detected in one allele. The variant does not cause amino acid substitution. Thus, it was considered that there was no oncogenic mutation in KIT and PDGFRA genes in this tumor.
This tumor consisted predominantly of round cells with a modest amount of eosinophilic to granular cytoplasm, irregular nuclear contour, and granular to vesicular chromatin with variably prominent nucleoli. Neoplastic cells were arranged in a nest-like structure compartmentalized by delicate vasculature. Although the current case conformed exactly to the morphological definition of high-grade ESS, the mitotic activity was inconspicuous. Immunohistochemically, c-kit and cyclin D1 are considered to be critical markers in diagnosing high-grade ESS [5, 6]. While the cell membrane and cytoplasm were positive for c-kit in the current case, there was no nuclear staining of cyclin D1. The diffuse positive signals for ER and PgR found in this case are also uncommon in high-grade ESS. The tumor cells were positive for some smooth muscle and myogenic markers including αSMA, muscle-specific actin, and heavy caldesmon, which have not been previously reported in high-grade ESS . These immunophenotypes might indicate epithelioid leiomyosarcoma rather than high-grade ESS.
In addition to morphological and immunohistochemical findings, molecular biological investigations offer a sophisticated approach that provides critical information for accurately diagnosing some types of bone and soft tissue tumors. Lee et al. reported that high-grade ESS typically harbors a YWHAE-NUTM2 fusion gene . The current case harbored 18% of YWHAE gene rearrangement. Conversely, the frequencies of NUTM2A and NUTM2B split signals were far lower than that of YWHAE. Although a small number of split signals is considered to be sufficient evidence of gene rearrangement in the diagnosis for some types of tumors, a relevant threshold of YWHAE split signals for diagnosing high-grade ESS under the current concept is reported to be 20% . Furthermore, YWHAE gene rearrangement may not be a specific finding for high-grade ESS. It was reported that translocation of t(10;17), including the YWHAE gene, was detected in a uterine sarcoma that was diagnosed as a poorly differentiated uterine tumor with t(10;17) translocation and neuroectodermal phenotype . The c-kit positivity seen in the current case might possibly be suggestive of a uterine GIST. However, the results of direct sequencing revealed that there was no mutation in exons 9, 11, and 13 of the KIT gene or in exon 18 of the PDGFRA gene in the tumor. Based on all these findings, the tumor was designated as uterine epithelioid leiomyosarcoma with c-kit expression and YWHAE gene rearrangement.
In conclusion, the tumor in this case seems quite instructive, showing a potential diagnostic pitfall of uterine sarcoma with epithelioid morphology. The tumor had some immunohistochemical features of leiomyosarcoma, high-grade ESS, and uterine GIST. In addition to the conventional practices for pathological diagnosis, molecular biological analysis led to a more definitive diagnosis. Interestingly, this uterine sarcoma exhibited unusual gene rearrangement for leiomyosarcoma. Accumulation of additional cases may enable an appropriate evaluation of prognosis, better treatment, and a novel paradigm for this disease.
Endometrial stromal sarcoma
Fluorescence in situ hybridization
Gastrointestinal stromal tumor
Availability of data and materials
There are no additional supporting data available.
TK and SS carried out histopathological evaluation and drafted the manuscript. RW performed direct sequencing. NK, YI, TS, HF, and HH assisted with the pathological analysis. RT, MI, ME, and TS collected the clinical and surgical data. TH conceived of the study and participated in the design, and the preparation of the manuscript. All authors read and approved the final manuscript.
There are no conflicts of interests in this study.
Consent for publication
The patient gave general consent for the use of their tissue/data for research purposes as authorized by the Institutional Review Board of Sapporo Medical University Hospital (282–65). Written informed consent for publication of clinical details and clinical images was obtained from the patient. A copy of the consent form is available for review by the Editor of this journal.
Ethics approval and consent to participate
The ethical approval and documentation for a case report was waived with approval of the Institutional Review Board of Sapporo Medical University Hospital.
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