Rare gynecological entity: malignant cervical PEComa (perivascular epithelioid cell differentiation tumour) - challenges in diagnosis, treatment and surveillance

ABSTRACT

Perivascular epithelioid cell tumors constitute a family of mesenchymal tumors characterized by the concomitant expression of melanocytic and muscular markers. Gynecological perivascular epithelioid cell tumors are rare, encompassing about 25% of cases. Studies demonstrate an even rarer occurrence in the uterine cervix. In this article, we report a case of malignant perivascular epithelioid cell tumors of the uterine cervix in a young patient, managed with total hysterectomy with unilateral salpingo- oophorectomy (due to suspected neoplasic involvement of the right ovary) and bilateral pelvic lymphadenectomy. Due to limited data, diagnosing these tumors is challenging. Given the uncertain biological behavior of this neoplasm, they should be considered potentially malignant and require long-term follow-up, despite the potential for late local recurrence and distant metastases. Surgical treatment involving complete resection of the lesion with clear margins remains the recommended option for this type of tumor until more consistent evidence can support adjuvant treatments.

RESUMO

Os tumores perivasculares de células epitelióides constituem uma família de tumores mesenquimais caracterizados pela expressão concomitante de marcadores melanocíticos e musculares. Tumores perivasculares de células epitelióides ginecológicos são raros, abrangendo cerca de 25% dos casos. Estudos demonstram uma ocorrência ainda mais rara no colo uterino. Neste artigo, relatamos um caso de tumor perivascular de células epitelióides maligno do colo uterino em paciente jovem, tratado com histerectomia total com salpingo-ooforectomia unilateral (por suspeita de envolvimento neoplásico do ovário direito) e linfadenectomia pélvica bilateral. Devido aos dados limitados, diagnosticar esses tumores é um desafio. Dado o comportamento biológico incerto desta neoplasia, devem ser consideradas potencialmente malignas e requerem seguimento a longo prazo, apesar do potencial de recorrência local tardia e metástases à distância. O tratamento cirúrgico envolvendo ressecção completa da lesão com margens claras continua sendo a opção recomendada para esse tipo de tumor até que evidências mais consistentes possam apoiar tratamentos adjuvantes.

Keywords:

Uterine cervical neoplasms - Perivascular epithelioid cell neoplasms - Hysterectomy

Descritores:

Neoplasias cervicais uterinas - Neoplasias perivasculares de células epitelióides - Histerectomia

INTRODUCTION

Perivascular epithelioid cell tumors, or PEComas, represent a family of mesenchymal tumors characterized by the simultaneous expression of melanocytic and muscular markers.[1] Perivascular epithelioid cells were initially described in renal angiomyolipomas by Apitz, in 1943.[2] However, the concept of PEComa was introduced by Bonetti et al., in 1992[3] - a tumor composed of cells with an epithelioid appearance, clear eosinophilic cytoplasm, and perivascular distribution.[4] Cells in PEComas are organized around blood vessels and appear to be part of their wall, sometimes infiltrating the smooth muscle of small to medium-sized vessels. There are several hypotheses attempting to explain the origin of these cells, ranging from undifferentiated neural crest cells expressing both melanocytic and smooth muscular phenotypes, myoblastic cells undergoing molecular alterations leading to melanocytic marker expression, to an origin in pericytic cells.[5]

These tumors can arise in various anatomical sites, including the kidney, lung, bladder, prostate, pancreas, liver, falciform ligament/round ligament of the liver, breast, skin, eyes, skull base, colon, soft tissues, retroperitoneum, and the female genital tract.[5] The differential diagnosis of these tumors is broad, comprising benign tumors like leiomyomas and lipomas, as well as malignant tumors including malignant melanoma, clear cell carcinoma, leiomyosarcoma, and liposarcoma.[6]

Gynecological PEComas are rare, constituting approximately 25 to 30% of cases of this tumor type, with the uterine body accounting for the majority of cases (close to 72% in the retrospective study by Liu et al. (2019).[7] Studies demonstrate an even rarer occurrence in the uterine cervix - approximately 10.5% of gynecological PEComas are located in the cervix.[5]

This study aims to report a case of malignant PEComa of the uterine cervix, focusing on the rarity of this tumor type, the proposed surgical treatment, the pathologist’s importance in the differential diagnosis of this neoplasm, and the follow up of this patient.

CASE DESCRIPTION

A 34-year-old female patient was referred by a gynecologist to a surgical oncology service due to vaginal bleeding and an expansive mass in the uterine cervix evolving over 5 months.

The patient had 2 previous gestations. She was using oral contraceptives and had a history of discontinuing them due to vaginal bleeding. A colpocitology had been previously conducted (1 month prior to the consultation with surgical oncology team), revealing cervical intraepithelial neoplasia (CIN) II/III. Upon speculum examination, a large friable, bleeding, exophytic mass with necrotic areas in the uterine cervix was observed, occupying the entire lateral aspect of the vaginal canal, rendering the cervical orifice unidentifiable.

Biopsy samples were collected from the mass, and the histopathological report indicated a poorly differentiated carcinoma, featuring clear and signetring-like cells, requiring immunohistochemistry (IHC) to confirm the lesion’s origin.

IHC was positive for estrogen receptor (EP1), desmin (D33) in rare cells, focal alpha-smooth muscle actin (1A4), weak and focal melan-A (A 103), HMB45, TFE3 (EP285 clone), weak p63 (DAK-p63 clone) in rare cells, vimentin (V9), and Ki-67 (MIB-1) in approximately 20% of cells, consisting with PEComa.

Pelvic magnetic resonance imaging (MRI) revealed a solid ovoid lesion measuring 5 cm in diameter, involving the uterine cervix and extending approximately 3 cm into the vaginal canal and no signs of parametria, rectum or bladder infiltration. ([figures 1] and [2]). There was no evidence of involvement of lymph nodes involvement. Complementary image exams including chest computed tomography (CT) and upper abdominal MRI were performed for staging, indicating no evidence of distant metastasis. Colonoscopy showed no remarkable findings.

Figure 1. Sagittal MRI section of the pelvis showing an expansive lesion in the uterine cervix, ovoid, in continuity with the vaginal vault, without evidence of involvement of the parametrium and regional lymph nodes.

Figure 2. Axial MRI section of the pelvis showing an expansive lesion in the cervix, with a cleavage plane with the bladder and rectum.

The patient was submitted to surgical treatment. The initial idea was preserve both ovaries due to patient age and histology, but in the transoperative it was observed that the right ovary had an increase in volume and a suspicious appearance for neoplastic infiltration, despite the normal appearance at MRI. We performed a total hysterectomy with unilateral salpingo-oophorectomy and bilateral pelvic lymphadenectomy ([figures 3]). The histopathological report of the surgical specimen revealed a poorly differentiated neoplasm with an epithelioid variant, measuring 5.5 x 4.3 cm, consistent with PEComa. None of the lymph nodes removed during the procedure showed neoplastic involvement - 10 left iliac lymph nodes and 14 right iliac lymph nodes. The surgical margins were free from neoplasia.

Figure 3. Product of total hysterectomy with unilateral salpin- go-oophorectomy and bilateral pelvic lymphadenectomy.

Postoperatively, the patient showed good progress and was referred for consultations with clinical oncology and radiation oncology to discuss adjuvant therapy options. It was decided not to proceed with any form of adjuvant therapy for this patient, who continues under clinical follow up, showing no evidence of disease after 28 months.

DISCUSSION

Gynecological PEComas are rare, with the majority being sporadic tumors, and a smaller percentage associated with complex tuberous sclerosis (CTS). PEComas of the uterine cervix are even rarer - only 16 cases have been reported in the literature until now.[1] The present case represents the 17^th case of this tumor type described in the literature, and [Table 1] summarizes the main characteristics of all these reported cases.

Table 1. Cervical PEComa cases reported until now in literature.

Cases	Age	History of CTS/gene mutation	Tumor size	Folpe’s criteria for agressive behavior	Treatment	Follow up
Case 1	41	Yes	2.2 cm	None	Total histerectomy with bilateral salpingo- oophorectomy	35 months, without evidence of recurrence
Fadare et al., (2004)[8]			Intraabdominal PEComatosis
Case 2	48	No	2 cm	High nuclear grade	Local excision and adjuvante radiotherapy	21 months, without. evidence of recurrence
Folpe et al., (2005)[9]
Case 3	28	No	3 cm	None	Histerectomy and lymphadenectomy	36 months, without evidence of recurrence
Folpe et al., (2005)[9]
Case 4	25	No	Cervical anterior lip ulceration	Infiltrative margins	Total histerectomy with bilateral salpingo- oophorectomy and lymphadenectomy	NI (no information)
Azad et al., (2006)[10]
Case 5	24	No	Cervical membranous tissue	Infiltrative margins	Local excision	2 early cervical recurrences - 4 months after the first procedure, and 7 months after the second procedure
Yamamoto et al., (2010)[11]
						12 months after the thirdprocedure: without evidence of recurrence
Case 6	46	No	3-4 cm	None	Total histerectomy with bilateral salpingo- oophorectomy + radiotherapy (external beam radiation therapy - EBRT) + immunotherapy	36 months, without evidence of recurrence
Bradshaw et al., (2010)[6]
Case 7	61	No	9 cm	Size > 5 cm	mTOR inhibitors	Death (8 months)
Wagner et al., (2010)[12]			Pulmonary metastasis at diagnosis
Case 8	59	Yes	Non-specified	NI	Total histerectomy with bilateral salpingo- oophorectomy	NI
Lim et al., (2011)[13]
Case 9	52	No	12 cm	Vascular invasion, necrosis, high nuclear grade	Pelvic exenteration with uterus, vagina, bladder and anal canal resection + adjuvante radiotherapy (28 fractions)	12 months, without evidence of recurrence
Natella et al., (2013)[14]
Case 10	57	NI	3.3 cm	Multiple bizarre giant cells, necrosis, mitotic index 2MF/5QHPF	Total histerectomy with bilateralsalpingo-oophorectomy	NI
Zhang et al., (2013)[15]
Case 11	41	Yes	4 cm Intraabdominal PEComatosis	Infiltrative margins	Total histerectomy with bilateralsalpingo-oophorectomy	36 months, without evidence of recurrence
Çelik et al., (2014)[16]
Case 12	34	No	9 cm	Size > 5 cm, necrosis, infiltrative margins	Mass resection	Local recurrence after 2 months
Liu et al.,(2014)[17]		[*] TFE3 mutated				Metastatic pelvic lymph nodes after 5months
Case 13	51	No	2.8 cm	None	Total histerectomy with bilateralsalpingo-oophorectomy	SI
Tajima and Koda, (2015)[18]
Case 14	43	No	3 cm	None	Histerectomy	36 months, without evidence of recurrence
Kovac et al., (2018)[19]		[*] TFE3 mutated
Case 15	57	No	11 cm	Size > 5 cm, infiltrative margins, high nuclear grade, necrosis, mitotic index > 4 MF/10HPF	Total histerectomy with bilateral salpingo-oophorectomy and pelvic lymphadenectomy	6 months, without evidence of recurrence
Mateva et al., (2019)[1]
Case 16	55	SI	3 cm	None	Total histerectomy with bilateral salpingo-oophorectomy	24 months, without evidence of recurrence
Tang et al.,(2023)[20]
Case 17	34	SI	5.5 cm	Size > 5 cm	Total histerectomy with unilateralsalpingo-oophorectomy and bilateral pelvic lymphadenectomy	28 months, without evidence of recurrence
Our case

NI = No information; CTS = Complex tuberous sclerosis.

The first cervical PEComa was described by Fadare et al., in 2004,[8] who also introduced the term “PEComatosis”. PEComatosis refers to the occurrence of perivascular epithelioid cell clusters on the peritoneal surface, likely due to de novo proliferation.

While most PEComas are benign, a subgroup demonstrates aggressive behavior.[1] Histological findings commonly associated with a more aggressive behavior of the neoplasm include tumors larger than 5 cm, infiltrative growth pattern, high nuclear grade, and more than 1 mitosis per 50 highpower fields (1M/50HPF). Malignant gynecological PEComas can spread to the vagina, uterine tubes, ovaries, bladder, and ureters, and can metastasize to the lungs, and less frequently to the liver, intestines, lymph nodes, and peritoneal cavity.[4],[5] They may also exhibit local recurrence, as described in a case report by Yamamoto et al. (2010).[11]

In 2005, Folpe et al.[9] analyzed 26 PEComas from soft tissues and gynecological sites and defined criteria for malignancy ([Table 2]), categorizing tumors as benign, uncertain malignant potential, or malignant. Folpe’s criteria are accepted in the World Health Organization (WHO) classification. WHO criteria for tumors of the female reproductive organs serve as parameters that impact the disease prognosis.[1],[9] Other criteria for assessing malignancy have been developed, such as Schoolmeester’s criteria (2014)[21] and the modification of Folpe’s criteria by Conlon et al. (2015).[22] Conlon et al.[22] compared the three criteria systems for assessing malignancy in PEComas and reported that Folpe’s criteria (both original and modified) demonstrated high sensitivity and negative predictive value when compared to Schoolmeester’s criteria. However, PEComas deemed malignant by Schoolmeester’s criteria exhibited earlier recurrences.[22]

Table 2. Criteria for malignance assessment in PEComas.

Category	Folpe’s criteria (2005)[9]	Schoolmeester’s criteria (2014)[21]	Folpe’s modified criteria -Conlon et al. (2015)[22]
Benign	None of below criteria: • Size equal or higher 5 cm • Infiltrative growth pattern • High nuclear and cellularity grade • Mitotic index > 1M/50HPF • Necrosis • Vascular invasion	Less than four below criteria: • Size equal or higher 5 cm • High nuclear grade • Mitotic index > 1M/50HPF • Necrosis • Vascular invasion	None or one below criteria: • Infiltrative margins • Size between 5 and 10 cm • Mitotic index 2-3M/50HPF • Lymphatic and vascular invasion
Uncertain malignant potential	One of below criteria: • Nuclear pleomorphism/giant multinucleated cells • Size equal or higher 5 cm		One of below criteria: • Isolated important atypia • Size > 10 cm • Mitotic index equal or higher than 4M/50HPF
Malignant	Two or more below criteria: • Size equal or higher 5 cm • Infiltrative growth pattern • High nuclear and cellularity grade • Mitotic index > 1M/50HPF • Necrosis • Vascular invasion	Four or more below criteria: • Size equal or higher 5 cm • High nuclear grade • Mitotic index > 1M/50HPF • Necrosis • Vascular invasion	Any grade of necrosis or two or more above criteria

Adapted from Mateva et al., (2019)1. 1M/50HPF = 1 mitosis per 50 high-power fields.

There is a correlation between the development of PEComas and tuberous sclerosis complex, a rare genetic disease that can lead to the formation of multiple tumors (mostly benign) in various parts of the body, including the brain, skin, kidneys, heart, eyes, and lungs. In tuberous sclerosis, a mutation occurs in the TSC1 and TSC2 genes, located on chromosomes 9 and 16, respectively. In PEComas, mutations in the TSC gene can also be found, with 27% in TSC1 and 73% in TSC2, both in cases related to tuberous sclerosis complex and sporadic cases.[16] The TSC genes are involved in regulating the PI3K/ mTOR signaling pathway, which may explain the promising results obtained in PEComa treatment with mTOR inhibitors such as sirolimus, temsirolimus, and everolimus.[5] The association with tuberous sclerosis is more significant for angiomyolipomas and lymphangioleiomyomatosis than for gynecologic and soft tissue PEComas.[6] In the present case, there was no investigation of somatic mutations in the patient’s tumor or searching for tuberous sclerosis complex, as she was attended within a context of a public health system with limited resources.

Another potential genetic alteration that may lead to the development of PEComas is the fusion/translocation of the TFE3 gene. These tumors typically affect younger patients without an association with tuberous sclerosis complex, displaying predominantly alveolar architecture and epithelioid cytology, low-grade nuclear atypia, rare mitoses, and minimal immunoreactivity to muscle markers.[5],[20] Liu et al. (2014)[17] reported a case of uterine cervix PEComa with TFE3 gene alterations in a 34-year-old patient who experienced local disease recurrence after resection and pelvic lymph node metastases, supporting the neoplasm’s more aggressive biological behavior. This raises questions about the inclusion of TFE3 fusion/translocation as criteria for a worse prognosis and a more aggressive course of the disease, increasing the likelihood of tumor malignancy. The true pathogenic contribution of TFE3 gene alterations in the context of PEComas remains uncertain, and due to its rarity, establishing therapeutic options based on this, as seen with TSC1 and TSC2 genes, becomes challenging.[17]

Histologically, PEComas exhibit clear or granular cytoplasm and typically organize in a perivascular pattern, concurrently expressing myogenic markers such as smooth muscle actin (SMA) and melanocytic markers (HMB-45 and Melan-A). They present as circumscribed masses with both solid and cystic components, with rare involvement of adjacent structures or organs.[4]

The clinical presentation is not specific, including symptoms such vaginal bleeding, pelvic/uterine masses, and pelvic and abdominal pain. Due to vaginal bleeding, cervical PEComa patients may also experience anemia.[4] It is important to consider that the patient’s signs and symptoms vary based on the tumor’s size, location, and potential metastases. [23] Uterine rupture and hemoperitoneum are rare presentations of this tumor type.[24] In this case, the patient presented with the most common symptom - vaginal bleeding, attributing it to the discontinuation of oral contraceptives. This symptom can be attributed to a lot of pathologies of female genital tract, which contributes to difficult and postpone the diagnosis.

PEComa constitutes a group of neoplasms with a challenging diagnosis, given their rarity and immunophenotypic and morphological overlap with other benign and malignant tumors.[6] On clinical examination, cervical PEComa may manifest as a solid, friable mass or a polypoid lesion.[5]

There is still limited data regarding colpocytology in cervical PEComa.[5] To date, only two cases of cytological diagnosis of cervical PEComa using conventional methods have been described in the literature.[20] Stone et al.[18] reported the presence of a uniform population of loosely cohesive cells with clear, fragile cytoplasm, uniform nuclei with finely stippled chromatin, and a single prominent nucleolus in a cytological examination of a lesion later biopsied during conization and diagnosed as PEComa through immunohistochemistry (IHC).[5] The second case was reported by Tajima and Koda (2015)[18] in a 51-year-old patient with abnormal genital bleeding, exhibiting the same cytological findings previously reported by Stone et al.[18] Other methods are being explored to assist in the diagnosis of cervical PEComa. Tang et al. (2023) [20] reported a case of cervical PEComa in a 55-year-old patient initially identified through liquid-based cytology, subsequently confirmed through biopsy with histopathological analysis on paraffin block, IHC, and fluorescence in situ hybridization (FISH). In liquid-base cytology, the findings were similar to those in conventional cytology reported by Stone et al.[18] and Tajima and Koda (2015),[18] with atypical cells showing minimal cohesion, arranged individually or in clusters, exhibiting epithelioid morphology, abundant clear cytoplasm, and oval or round nuclei with finely stippled chromatin.[20]

Regarding imaging studies, on ultrasonography, cervical PEComa can be characterized by a heterogeneous area with well-defined margins or a hyperechoic appearance without a clear cleavage plane with the adjacent uterus and rich central vascularity.[5] On CT, malignant PEComas may appear as a hypodense or isodense mass without contrast, but with significant homogeneous or heterogeneous enhancement after contrast administration.[24] MRI provides better definition of the lesion’s internal structure,[5] revealing a heterogeneous hypointense mass on T1 and iso- or hyperintense on T2.[24] Natella et al. (2013)[14] reported the use of positron emission tomography-computed tomography (PET-CT) with 18-FDG (fluorodeoxyglucose) to complement local staging and exclude distant metastases in a patient with a huge cervical PEComa.[14] PET-CT can also be useful in assessing treatment response and follow up of patients with malignant PEComas, though data in the literature are scarce.[24]

The differential diagnosis of uterine PEComas is broad and includes mesenchymal neoplasms with epithelioid characteristics, with emphasis to smooth muscle tumors, endometrial stromal sarcomas, and malignant metastatic melanoma.[24]

The most effective treatment is not well-established yet due to the rarity of cervical PEComa.[20] Another challenge in therapeutic planning for this type of tumor is that the majority are diagnosed postoperatively.[7] Complete surgical resection with clear tumor margins is considered the optimal therapeutic approach; however, there is heterogeneity in the proposed surgical procedures in the literature, ranging from local resections to pelvic exenteration, as described in Table 1. Total hysterectomy with or without bilateral salpingo-oophorectomy should be considered in patients with PEComas localized in the cervix or spreading to it.[1],[6] In young patients with reproductive desires, fertility-preserving surgery may be a surgical treatment option, as described by Yamamoto et al. (2010)[11] and our report. Larger tumors may require more extensive resections, as reported by Natella et al. (2013),[14] who performed pelvic exenteration due to a bulky tumor of about 12. The optimal treatment choice for recurrent or metastatic disease remains uncertain.[7]

Regarding adjuvant therapy with chemotherapy and radiotherapy, studies have not consistently demonstrated benefits in this scenario.[19] Some sporadic and syndromic tumors show inactivation of TSC1 and TSC2 genes with subsequent mTOR pathway activation. These tumors may respond to mTOR inhibitor therapy, such as sirolimus and everolimus, especially in the context of metastatic disease.[1],[6],[12]

Due to the rarity of these tumors, predicting their clinical behavior becomes challenging.[7] Despite limited data, cervical PEComas should be regarded as tumors with uncertain malignant potential and require long-term follow-up due to the potential for local recurrence and distant metastases,[1] which can occur several years (7-9 years) after surgical resection.[14] Regarding the chosen imaging method for monitoring these patients, there is still limited data. Mateva et al. (2019)[1] reported the follow-up of such tumors using chest, abdomen, and pelvic CT every 6 months.

CONCLUSION

There are few reported cases of cervical PEComa in the literature, with the present report documenting 17 cases. Due to limited data, diagnosing these tumors poses a challenge, and given the uncertain biological behavior of this neoplasm, they should be considered of uncertain malignant potential. These tumors require long-term follow-up, notwithstanding the potential for late local recurrence and distant metastases. Surgical treatment, involving lesion resection with clear margins, remains the recommended therapeutic option for this type of tumor until more consistent evidence can support adjuvant approaches with chemotherapy, radiotherapy, and targeted therapy.

AUTHORS’ CONTRIBUTIONS

ASA Collection and assembly of data, Conception and design, Data analysis and interpretation, Final approval of manuscript, Manuscript writing, Provision of study materials or patient

FVK Collection and assembly of data, Conception and design, Data analysis and interpretation, Final approval of manuscript, Manuscript writing, Provision of study materials or patient

RVK Collection and assembly of data, Conception and design, Data analysis and interpretation, Final approval of manuscript, Manuscript writing, Provision of study materials or patient

DRB Collection and assembly of data, Conception and design, Data analysis and interpretation, Final approval of manuscript, Manuscript writing

LFV Manuscript writing

STT Conception and design, Final approval of manuscript, Manuscript writing

Conflict of Interests

The authors declare no conflict of interest relevant to this manuscript.

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Publication History

Received: 04 December 2023

Accepted: 05 February 2024

Article published online:
02 May 2024