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Menopause Review/Przegląd Menopauzalny
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vol. 15
Original paper

Leiomyoma and leiomyoma cellulare of the fallopian tube: review of the literature and case reports

Dobrosława L. Sikora-Szczęśniak

Menopause Rev 2016; 15(3): 143-147
Online publish date: 2016/11/15
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Leiomyoma cellulare (LC) is the most common benign tumor of the female genital tract, including the uterine body. It is a benign non-epithelial, mesenchymal monoclonal tumor of smooth muscle cells and a framework of fibrous connective tissue [1, 2]. Uterine LC occurs with 5% frequency [3].
These tumors develop as genetically abnormal clones of cells originating from one precursor cell where the original mutation took place. Multiple leiomyomas do not belong to the same clone; each develops irrespectively of the others [4]. Their more common occurrence in first-degree relatives suggests genetic background of the disease [5].
Recently, more and more attention has been paid to the role of genes (tuberous sclerosis complex gene – TSC) in the etiology of malignant and benign tumors. Lost function of those genes manifested as a decreased level of TSC gene product, i.e. tuberin was observed in 50% of cases of uterine leiomyomas, which suggests genetic etiology of the disease [6-8].
Clinically LC appears as solid nodules of large smooth muscle cells and their nuclei without atypia, of low mito­tic activity up to 5 division figures/10 HPF, with scarce connective tissue elements. It is often referred to as cellular leiomyoma [9-11].
On postoperative macro- and microscopic examination, the mass of removed LC tumors and uteruses was considerably larger compared to leiomyomas [12].
Leiomyoma of the fallopian tube originates from the myosalpinx or the cells of the blood vessels supplying the fallopian tube. In most cases it is located in the isthmus, rarely in the ampulla, but it is also found as myoma nascens. Similarly to uterine leiomyomata, the leiomyoma of the fallopian tube may be located submucosally, intramurally or subserosally. When large enough or in statu nascendi they tend to twist or degenerate [13, 14].
The paper aims at reviewing literature reports on leiomyoma of the fallopian tube and its variant, leiomyoma cellulare. Moreover, it presents two case reports of the patients operated on in our ward. Microscopic histological examination found leiomyoma parvum of the left fallopian tube (case 1), and leiomyoma cellulare partim epithelioides of the right fallopian tube (case 2).

Material and methods

The paper reviews accessible research articles published in the last decades on the cases of leiomyoma of the fallopian tube, and a case of LC of the fallopian tube. The analysis focused on:
• preoperative diagnostic methods and preoperative dia­gnosis,
• patient’s age, body mass index (BMI), and obstetric history,
• methods of treatment and extent of surgery,
• results of surgical treatment.
Moreover, we present two case reports of the patients operated on in our ward: one patient had leiomyoma of the left fallopian tube, and the other LC of the right fallopian tube; both diagnoses were made on microscopic histopathological examination.


Leiomyoma of the fallopian tube is rare and often incidentally detected at surgery or autopsy [15]. In the majority of cases preoperative diagnosis is sporadic as the disease course is asymptomatic, and those tumors are singular, small size, and unilaterally located nodules [15, 16].
When the mass of a leiomyoma located in the fallopian tube is larger, the so called “effect of mass” can cause additional symptoms from the urinary bladder, ureters or the alimentary tract [17]. Moreover, torsion, or degeneration is unlikely to be found until surgery and histopathological examination [14].
Imaging techniques, such as transvaginal ultrasonography (USG) Doppler, computed tomography (CT) and magnetic resonance imaging (MRI) are useful for preoperative diagnostics as they can detect a leiomyoma mass in the fallopian tube, the location other than the uterus. However, the final diagnosis is made intraoperatively by results of histological examination [16].
The age of patients with leiomyoma of the fallopian tube, whose cases are presented in the papers, ranged from 27 to 44 years [13-20]. The mean age of the patients in the group with uterine leiomyomas and leiomyomas and endometriosis was 49.1 years [3].
The age of the patients operated on in our ward, of 68 and 56 years, was higher than the mean age of 45.6 years noted in the group of patients with uterine LC [3].
Ozkan et al. presented a case of a 70-year-old patient with LC of the fallopian tube [21].
The risk factors include nulliparity, advanced age, obesity, and family history of leiomyomas [17].
The operative technique and extent of the operation depended upon the patient’s age, size of the lesion in the fallopian tube and the result of intraoperative histo­pathological examination. Laparoscopy was used as a diagnostic technique to localize the mass and for intraoperative histopathological examination of the sample.
The large mass of the diseased fallopian tube and coexisting diseases affecting the internal genital organs were decisive for the extent of the operation, sometimes conversion of laparoscopy into laparotomy was necessary [13].

Case reports of the patients operated on in our ward

Case 1

The patient, G.K., 68 years, was admitted for uterine leiomyomas and recurrent uterine bleeding; menopause at 55, four natural deliveries.
Preoperative diagnosis and patient’s medical history and examination found obesity (class I, body mass 67 kg, BMI = 32.80). Additionally, the patient was on medication for hypertension and coronary heart disease.
Surgical operation: hysterectomy with bilateral adnexa by laparoscopic approach was performed on 3 De­cember 2002.
Findings of postoperative histological examination of the material:
• the uterine body – Endometrium senile cysticum. Endometriosis diffusa. Leiomyomata intramuralia et subserosa unius cellulare corporis uter,
• the uterine cervix – Erosio glandularis partim epidermisata cum inflammatione. Ovula Nabothi,
• left appendages – Cystis simplex ovarii atrophici. Leiomyoma parvum oviducti,
• the right appendages – Ovarium. Oviductus.
The patient was discharged on the 6th day following the operation.

Case 2

The patient, K.T., 53 years, admitted for a tumor in the right appendages on 18 March 2015.
History findings: regular menstruation from the age of 14 to 53; five natural deliveries. Preoperative diagnosis, patient’s history and physical examination revealed obesity (class II, body mass 95 kg, BMI = 37.11); additionally the patient was on medication for hypertension, type 2 diabetes, and schizophrenia.
Laboratory tests were done and pharmacological treatment of concomitant diseases continued as consulted by specialists.
Laboratory results found temporary elevated blood glucose 173 mg/dl. Complete blood count (CBC), electrolytes, kidney parameters and blood coagulation parameters were within normal range. CA125 23.16 U/ml within the normal range.
Gynecological examination findings: vaginal section of the uterine cervix normal, muco-serous fluid scarce. The uterus and appendages difficult to examine due to the patient’s obesity.
Ultrasound scan (Fig. 1): the uterus body not enlarged, size of 5 × 3 × 3 cm. Endometrium 5.4 mm thick. On the right side, a cyst 55 × 50 mm in diameter filled with thick fluid, the appendages on the left side normal.
Preoperative diagnosis of the cyst of the right fallopian tube was made, and the patient was qualified for laparoscopy on 24 March 2015.
Surgical operation – in the course of laparoscopy, the operator decided on conversion to minilaparotomy because of the tumor size of 80 × 60 × 55 mm. The right appendages with the tumor of the right fallopian tube were excised, and left salpingectomy was performed.
Intraoperative examination found a benign lesion of the right fallopian tube – tumor of 80 × 60 × 55 mm, lobular, grayish, of smooth surface, growing at the terminal part the fallopian tube; the fallopian tube unwidened, along it numerous spotty whitish cyst-like nodules filled with whitish fluid.
Histopathological examination under microscope (No 996010-7/15) found:
• tumor of the right fallopian tube – Leiomyoma cellulare partim epithelioides, of atypical nuclei, mitotic index 0,
• right fallopian tube – Oviductus,
• right ovary – Ovarium,
• left fallopian tube (No. 995981/15): fallopian tube 70 cm – long, 5 mm in diameter, with singular minute cysts on the surface – Oviductus et cystis serosa paraoviducti.
The patient was discharged from the ward on the 4th day following the operation. The postoperative course was uneventful in all the cases described in the literature, as well as in the patients operated on in our ward.


There are only few reports on leiomyoma of the fallopian tube in the literature as its incidence is defined as extremely rare [13, 16, 18, 20].
In their review of the literature, Mroueh et al. quoted fewer than 100 cases of leiomyomas of the fallopian tubes [22]. Since then several researchers have discussed those cases, including one of LC of the fallopian tube [13-21, 23, 24]. It is difficult to evaluate the frequency and risk of LC of the fallopian tube as the number of cases is very small [17].
The cases of LC variant located in the extrauterine region are really incidental. There are only two cases described in the Polish literature [3, 25]. Among the leiomyomas and LC cases, LC in the extrauterine region and LC in the uterine cervix accounted for 0.34% and 6.25%, respectively [3].
As seen in the literature review, the presented case of LC of the fallopian tube is the second one reported [21].
In the discussed cases of leiomyoma of the fallopian tube, the patients’ age was 27, 32, 34, 35, 39, 41, 44, and 44 years [respectively 13-20].
The mean age in the group of the patients with leiomyomas and leiomyomas with endometriosis was 49.1 yrs [3]. Thus, the age of the patients operated on in our ward, of 68 and 56 years, was higher compared to the mean age of 45.6 years [3].
The patient with LC of the fallopian tube, whose case is presented by Ozkan et al., was 70 [21].
Yang et al. state that leiomyomas of the fallopian tube are generally small nodules located unilaterally [16]. In the case presented above, the tumor mass was considerably large compared to the size of the fallopian tube itself. Ozkan et al. found LC of the fallopian tube of 130 × 90 × 70 mm [21].
Takongmo et al. and Cisse et al. described detected leiomyomas of the fallopian tube as “giant” [13, 17].
Moreover, torsion of leiomyomas of the fallopian tube and degeneration were also reported [13-15, 19, 24].
There are also cases of uterine pregnancies and a case of ectopic pregnancy (in the fallopian tube) in the patients with leiomyoma of the fallopian tube [17, 22, 23]. In the case of giant tumor in the right fallopian tube, the pregnancy was spontaneously aborted [17].
The operative method and technique were commensurate with the size of the diseased fallopian tube, concomitant problems affecting internal genital organs, and the result of intraoperative histopathological exa­mination.
When the fallopian tube affected by LC ruptured and bleeding to the peritoneal cavity occurred, emergency laparotomy was performed [21].
Preoperative diagnostics emphasize the importance of imaging techniques (USG Doppler, CT, MRI) for the diagnosis of leiomyoma of the fallopian tube [16]. If suspected, the diagnosis is confirmed by laparoscopy and results of intraoperative histopathological examination. That is what exactly happened in the presented case when it was necessary to convert laparoscopy into minilaparotomy. Similar decisions were taken in other presented cases, too [16, 19].
Sometimes preoperative imaging is not enough to define the nature of a lesion, however it is generally very useful to locate the change.
In the above-presented cases, preoperative diagnosis considered mesenteric tumor, abdominal tumor, tumor of the pelvis minor, bleeding to the peritoneal cavity, torsion of the subserosal uterine leiomyoma [13, 14, 17, 19, 21].
In the case of our patient, the initial diagnosis was ovarian cyst.
Concomitant diseases of the genital organs that are the reason for operation can pose other difficulties in detecting leiomyoma of the fallopian tube by imaging techniques, especially if the lesion is small. That happened in case 1 presented above.
It supports incidental detection of the majority of cases at surgery or autopsy [14-16, 18].
Genetic research by Lobel et al. found that larger leiomyoma uteri tumors more frequently contained cells of abnormal karyotype in comparison to smaller tumors [26].
Guan et al. suggested that LC tumors were smaller in diameter compared to leiomyosarcoma (LMS) [27].
The analysis of the reviewed papers suggests that LC is not detected until histopathological examination of the postoperative material has been done.
To differentiate between LC and sarcoma stromale and leiomyosarcoma immunohistochemical methods must be applied, e.g. expression of desmin, h-caldesmon, CD10, and CD44v3 [28, 29].
The researchers believe that LC is not a transient form of leiomyosarcoma. Guan et al. examined 78 patients with LC over a longer period, and in 41 cases the tumor did not transform into malignancy [27].
However, some authors consider the nature of LC as “borderline” pathology and recommend longer clinical observation of those patients. Another fact, which has to be considered, is that some of the cases transformed into rare malignant histological subtypes of leiomyoma, e.g. lipoleiomyoma [30].
When LC was detected without concomitant malignancies in the genital organs, the patients did not require complementary treatment following the operation [27].
There were no postoperative complications observed in the cases quoted; the postoperative course of the patients operated on in our ward was uneventful, too.


The diagnosis of leiomyoma and LC of the fallopian tube, just like in other female genital organs, is not possible until microscopic histopathological examination has been done.


Author reports no conflict of interest.


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