Primary vaginal Ewing's sarcoma or primitive neuroectodermal tumor in a 17-year-old woman: a case report
© Rekhi et al; licensee BioMed Central Ltd. 2010
Received: 23 October 2009
Accepted: 17 March 2010
Published: 17 March 2010
Primary Ewing's sarcoma or primitive neuroectodermal tumor of the genital tract of women is uncommon. Rarer still is its occurrence in the vagina, with only five cases described so far. Out of these, only one case was confirmed using molecular analysis.
We present an extremely rare case of Ewing's sarcoma or primitive neuroectodermal tumor in a 17-year-old Indian girl. She presented with a vaginal mass that was initially diagnosed as a malignant round cell tumor. Immunohistochemistry showed diffuse positivity for vimentin, membranous positivity for MIC2, and positivity for BCL2 and FLI-1. On the other hand, she was negative for cytokeratin, epithelial membrane antigen, desmin, Myo D-1, myogenin and smooth muscle actin. A diagnosis of primitive neuroectodermal tumor was thus offered. Furthermore, a molecular analysis of our patient using reverse transcription-polymerase chain reaction technique showed positivity for t(11; 22) (q24; q12) (EWSR1-FLI1), thus confirming the diagnosis of a Ewing's sarcoma/primitive neuroectodermal tumor. Our patient was offered chemotherapy on Institutional protocol EFT 2001.
This is a rare case of primary vaginal Ewing's sarcoma or primitive neuroectodermal tumor, which was confirmed with molecular analysis, in the youngest patient known so far. This study reinforces the value of integrating morphological features with membranous MIC2 positivity, along with application of molecular techniques in objective identification of an Ewing's sarcoma or primitive neuroectodermal tumor at uncommon sites.
Primary extraosseous Ewing's sarcoma, also called primitive neuroectodermal tumor (PNET) is uncommonly documented as occurring in the genital tract of women, such as the uterine corpus, the cervix and the ovary [1–3]. The vagina is a rare site for the occurrence of a primary Ewing's sarcoma and/or PNET, with only five cases documented so far, including a single case confirmed with molecular analysis [4–8]. We present a case of vaginal Ewing's sarcoma or PNET occurring as a rare tumor diagnosed in a 17-year-old girl. It reinforces the value of molecular analysis preceded by histomorphology and immunohistochemistry (IHC) in objectively confirming the presence of specific sarcomas at unusual sites.
A 17-year-old girl from central India presented with complaints of whitish, foul-smelling vaginal discharge with fragmented bits that she had been experiencing for a year prior to presentation. She had no history of any associated vaginal bleeding. Prior to presentation, she underwent alternative treatment but the symptoms had persisted. A month before she presented to our hospital, she was referred to us with acute urinary retention. She was catheterized. Her clinical examination showed that her general condition was fair. She had a Foley's catheter in situ and an enlarged uterus with pyometra. She underwent routine laboratory, radiological, and pathological investigations.
Her laboratory findings are as follows: low haemoglobin (Hb) level at 9 g/dl, low red blood cell count (RBC) at 3.32 (normal = 3.8 to 4.8 × 10 e12/L); low haemoatocrit at 26.8% (normal = 36% to 46%); low mean corpuscular volume (MCV) at 80.0 (normal = 83 to 10/FL). Meanwhile, her C-reactive protein value was high at 8.54 mg/dl (normal= < 1 mg/dl). She also had high serum lactate dehydrogenase (242 U/L) and alkaline phosphatase levels.
Our patient also underwent radiological investigations. Her magnetic resonance imaging (MRI) showed a soft tissue mass involving her anterior and posterior vaginal walls and her anterior sacrum. Her urinary bladder was displaced anteriorly. The mass was hyperintense on T2-weighted and hypointense on T1-weighted imaging. She had no pelvic lymphadenopathy. Her ureters were also identified along with her visualized bones. Her chest X-ray revealed no abnormality.
A computed tomography (CT) of her thorax showed a sub-centimeter-sized mediastinal node and multiple nodules in her bilateral lung parenchyma and subpleural location. Her pleural spaces, heart, great vessels, and bilateral bronchi were normal.
Her abdominal CT showed bilateral kidneys with pressure changes and with dilated ureters. Her other organs and biliary tree were normal. No lymphadenopathy was identified.
Biopsy material from our patient was then submitted for molecular analysis using ribonucleic acid (RNA) isolation and reverse transcription polymerase chain reaction (RT-PCR). Her total RNA was isolated from formalin-fixed, paraffin-embedded tissue sections (FFPE tissue) using a Recover All Total Nucleic Acid Isolation kit (Ambion, USA). The extracted RNA was then treated with RNase-free DNase I before cDNA preparation. Her RNA was then reverse transcribed into cDNA using the Superscript First strand synthesis system (Invitrogen). A total of 500 nanograms of her total RNA was briefly reverse transcribed into cDNA using random hexamers at 42°C for 50 min, which was then followed by 70°C for 15 min.
The synthesized cDNA from our patient was then treated with RNase H for 20 min at 37°C to remove the RNA-DNA hybrids. A total of 2 μl from the reaction was PCR amplified using EWS 22.3 forward primer (5'-TCC TAC AGC CAA GCT CCA AGT C-3') and FLI1 11.3 reverse primer (5'-ACT CCC CGT TGG TCC CCT CC-3') in a 20-μl reaction volume containing 10 pmol each of the forward and reverse primers, for a total of 20 μl PCR master mix (Qiagen, Germany). PCR conditions from her samples were as follows: 35 cycles of 94°C for 30 s, 65°C for 1 min, and 72°C for 1 min. Her amplified PCR products were checked in 10% polyacrylamide gel and stained with silver nitrate. Two positive controls (EWS-FLI1 type-I and type-II PCR product cloned into pTZ57R/T vector) and one water-only (no cDNA) negative control were included in each run. To check the quality and integrity of the cDNA, FOXO1A was amplified as a housekeeping gene (FKH-F: 5' CAT CCC CTT CTC CAA GAT CA 3'; FKH-R: 5' GCT GCC AAG AAG AAA GCA TC 3').
We then offered our patient a diagnosis of PNET, although we also considered a close differential diagnosis of synovial sarcoma. In view of the uncommon location of her mass, molecular studies were recommended.
Following our diagnosis of primary Ewing's sarcoma or PNET of the vagina, our patient was subjected to combination chemotherapy for 9 weeks based on institutional protocol for Ewing's family of tumors (EFT) 2001, including drugs such as vincristine (1.5 mg/m2), ifosamide (2.0 g/m2), etoposide (100 mg/m2), cyclophosphamide (600 mg/m2), doxorubicin (60 mg/m2), and actinomycin (1.0 mg/m2). The induction phase was followed by local treatment with radiotherapy (RT), during which our patient was found to be clinicoradiologically free of the disease. Following this, she was put on maintenance chemotherapy, including the aforementioned drugs. She was also put on regular follow-up examinations for the next seven months.
Ewing's sarcoma and primitive neuroectodermal tumor (PNET) are defined as round cell sarcomas that show varying degrees of neuroectodermal differentiation and are identified by light microscopy, IHC and electron microscopy. While Ewing's sarcoma lacks neuroectodermal differentiation, a PNET possesses it . Both, however, are characterized by a t(11; 22) (q24; q12) chromosomal translocation leading to a chimeric transcript EWS-FLI1 in 85% of reported cases. Its presence thus confirms a diagnosis of primary Ewing's sarcoma/PNET, especially at unusual sites where the index of suspicion is low .
Literature review of 6 cases of primary vaginal Ewing's sarcoma/primitive neuroectodemal tumor (PNET)
Vang et al.  (2000)
FOD (19 mo)
Farley et al. (2000)
FOD (48 mo)
Petkovic et al. (2002)
AWD (18 mo)
Liao et al. (2004)
VIM+, MIC2+, FLI1+, synaptophysin+, neuron specific enolase (NSE)+, S-100+
TAH, BSO+ CT
FOD (36 mo)
McCluggage et al.  (2007)
VIM+, MIC2+, FLI1-
Present case (2009)
VIM+, MIC2+, FLI1+, BCL2+
Our patient's biopsy revealed a malignant round cell tumor below an unremarkable mucosa. In view of this location, differential diagnoses included poorly differentiated carcinoma such as a small cell carcinoma and round cell sarcomas like a Ewing's sarcoma/PNET, monophasic synovial, and rhabdomyosarcoma. The presence of uniform cells with focal rosettes, however, made a diagnosis of rhabdomyosarcoma less likely. On IHC, diffuse positivity with vimentin and lack of CK, EMA, CK7 ruled out a carcinoma. Diffuse membranous MIC2 positivity was more in keeping with a Ewing's sarcoma/PNET than neuroendocrine carcinoma and a synovial sarcoma that also shows MIC2 and cytoplasmic expression.
Meanwhile, MIC2 positivity is also identified in rhabdomyosarcomas and lymphomas. However, the lack of desmin, myogenin and MyoD-1 ruled out rhabdomyosarcoma, while LCA negativity ruled out a diagnosis of lymphoma. In addition, FLI-1 positivity was also helpful even though its expression is noted in lymphomas, rhabdomyosarcomas and synovial sarcomas . While the former two were ruled out, additional bcl-2 positivity was more consistent with a diagnosis of synovial sarcoma. At the same time, bcl-2 positivity has also been documented in a subset of PNETs . Finally, a diagnosis of Ewing's sarcoma/PNET was confirmed on RT-PCR with positive EWSR1-FLI1 results. SYT-SSX for a synovial sarcoma was negative. In five cases documented so far, only one case of vaginal Ewing's sarcoma/PNET was confirmed through molecular analysis .
The value of identifying Ewing's sarcoma/PNET as the correct diagnosis is necessary in coming up with specific treatment for patients. Despite its aggressive behavior at osseous sites, this tumor responds to specific chemotherapy. All the cases documented so far have been subjected to chemotherapy with options of surgery ranging from wide excision to total abdominal hysterectomy [5–8]. Adjuvant RT has also been offered in two cases [5, 6]. After being diagnosed with Ewing's sarcoma/PNET, for the next seven months our patient completed the induction phase of chemotherapy and underwent local RT, during which she was found to be disease-free. She is presently on maintenance chemotherapy.
The treatment outcome for patients with primary vaginal Ewing's sarcoma/PNET has been favorable in so far as documented cases are concerned. No metastasis or causalities have also been reported [4–7]. In contrast, a neuroendocrine carcinoma, more commonly in post-menopausal women, has a relatively downhill course. Despite a size of ≥ 5 cm in three out of five documented cases, a superficial, mucosal location and a relatively younger age of occurrence are possible reasons behind a relatively better treatment outcome [6–8].
Our case report describes a rare site of primary vaginal Ewing's sarcoma/PNET in the youngest patient known so far. It reinforces the value of IHC, including membranous MIC2 positivity and with molecular analysis, in the objective identification of this sarcoma at unusual sites like the vagina. Correctly identifying tumor type enables clinicians to identify specific CT procedures as treatment mainstay. The identification and documentation of more cases with a clinicopathological index of suspicion, the confirmation of diagnosis using ancillary techniques, and the management and follow-up results would greatly contribute to the existing knowledge of diagnosis and outcome of PNETs developing at unusual sites.
Written informed consent was obtained from our patient for publication of this case report and any accompanying images. A copy of written consent is available for review by the Editor-in-Chief of this journal.
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