Abstract
Background
Uterine smooth muscle tumor of uncertain malignant potential (STUMP) is rare tumor, and regarded as sub-classification in uterine smooth muscle tumors between benign and malignant criteria. In this study, we evaluated characteristics of cases with STUMP diagnosis in a 10-year period.
Methods
We retrospectively evaluated medical records of patients with histopathological STUMP diagnosis in Istanbul Training and Research Hospital, a tertiary center. We analyzed preoperative demographic, clinical features and postoperative follow-up. Preoperative sonographic data were re-evaluated.
Results
The mean age was 42 years. One patient was postmenopausal, and five patients were premenopausal. All of them had a complaint of meno-metrorrhagia. We re-evaluated preoperative sonographic images of patients, and defined 83.3% as well-defined margins, 66.7% hyperechoic, 100% heterogeneous, 66.7% non-cystic, 50% calcification and 66.7% acoustic shadowing. Pathologic features showed mean number of mitosis 8, mild atypia 66.7%, and necrosis 33.3%. In a 24-year-old unmarried female patient with myomectomy, we detected recurrance of tumor in sonographic and MRI studies after 11 months, and confirmed the diagnosis via tru-cut biopsy. There was no relevance between sonographic findings and atypia, necrosis and mitosis. The recurrence was not in relationship with mitosis, degree of atypia and necrosis. We found no relevance between tumor diameter and mitosis, atypia, necrosis and recurrence.
Conclusions
STUMP is classified as an intermediate form, histopathologically so calling it benign or malignant for sure is not possible. Singulary, solidity, hyperechogenicity, heterogenecity and features of acoustic shadowing and margins can guide us to preoperative sonographic diagnosis. Recurrence/metastasis after many years from operation can be seen, and those patients should be followed long term.
Keywords: Uterine smooth muscle tumor, STUMP, Sonography
Introduction
Uterine smooth muscle tumor of uncertain malignant potential (STUMP) is a rare tumor.
Uterine smooth muscle tumors are classified as benign leiomyoma and malignant leiomyosarcoma regarding presence of tumor cell necrosis, cytological atypia and mitotic activity. STUMP is regarded in World Health Organization (WHO) classification as smooth muscle tumors between benign and malignant criteria [1].
STUMP is seen mostly in age of mid-forties, who has been operated with preoperative leiomyoma diagnosis. Risk factors and prognosis are not fully understood, but in long-term follow-up, there is a potential of recurrence or metastasis.
In this study, we evaluated prognosis, sonographic and clinicopathologic features of cases with histopathological STUMP diagnosis.
Materials and Methods
We retrospectively evaluated medical records of patients with histopathological STUMP diagnosis between 2005 and 2015 in Istanbul Training and Research Hospital, a tertiary center. We analyzed preoperative demographic, clinical and histopathological features, and postoperative follow-up. Preoperative sonographic data were re-evaluated.
SPSS 15.0 for Windows was used for statistical analysis. Descriptive statistics were identified as number and percentage for categorical variables, and mean, standard deviation, minimum and maximum for numeric variable. Comparison of two independent groups was made with Mann-Whitney U test. The ratio in two groups for categorical variables was analyzed with Fisher’s exact test. Numerical variables were analyzed by Spearman correlation analysis due to failure to fulfill the parametric test condition. Statistical significance level has been accepted as P < 0.05.
Results
Case-based features and their statistical analysis of six patients with STUMP diagnosis are presented in Tables 1 and 2. The mean age was 42 years. One patient was postmenopausal, and five patients were premenopausal. All of them had a complaint of meno-metrorrhagia. Mean gravida was 5.5, and mean parity was 3.5. We re-evaluated preoperative sonographic tumor images, and defined 83.3% as well-defined tumor capsule, 66.7% hyperechoic, 100% heterogeneous, 66.7% non-cystic, 50% calcification and 66.7% acoustic shadowing. We performed total abdominal hysterectomy (TAH) and bilateral salpingooophorectomy (BSO) in 66.7% and myomectomy in 33.3% of the patients. In the histopathology, mean tumor diameter was 9.4 cm, localization was intramural in 83.3%, mean number of mitosis was 8 (in 10 high power fields (HPF)), mild atypia in 66.7% and necrosis in 33.3%. Mean follow-up time was 63.4 months. We could not reach one patient postoperatively. In a 24-year-old nulliparous woman who had undergone myomectomy, we detected recurrance of tumor in sonography and MRI studies after 11-month follow-up, and confirmed the diagnosis via tru-cut biopsy.
Table 1. Case-Based Features.
Case 1 | Case 2 | Case 3 | Case 4 | Case 5 | Case 6 | |
---|---|---|---|---|---|---|
Age | 48 | 44 | 40 | 43 | 52 | 24 |
Gravida | 12 | 8 | 2 | 4 | 7 | 0 |
Parity | 5 | 6 | 2 | 4 | 4 | 0 |
Menopausal state | Post | Pre | Pre | Pre | Pre | Pre |
Complaint | MM | MM | MM | MM | MM | MM and pelvic pain |
Sonographic findings | ||||||
Number of tumor/myoma | 5 | 1 | 1 | 1 | 1 | 2 |
Margins of the tumor | Ill-defined | Well-defined | Well-defined | Well-defined | Well-defined | Well-defined |
Echogenicity | Mixed | Mixed | Hyperechoic | Hyperechoic | Hyperechoic | Hyperechoic |
Appearance | Heterogenous | Heterogenous | Heterogenous | Heterogenous | Heterogenous | Heterogenous |
Cystic form | + | + | - | - | - | - |
Calcification | - | + | + | - | - | + |
Acoustic shadowing | + | - | - | + | + | + |
Free fluid | - | - | - | - | - | - |
Pathology | ||||||
Procedure | TAH + BSO | TAH + BSO | Myomectomy | TAH + BSO | TAH + BSO | Myomectomy |
Tumor diameter (cm) | 3.5 | 8 | 7 | 20 | 10 | 8 |
Localization | Intramural | Submucous | Intramural | Intramural | Intramural | Intramural |
Number of mitosis (n/10 HPF) | 4 | 17 | 8 | 5 | 8 | 6 |
Atypia | Mild | Moderate | Moderate | Moderate | Mild | Moderate |
Necrosis | + | + | - | - | - | - |
Follow-up (months) | 120 | 119 | NR | 38 | 29 | 11 |
Recurrence | - | - | NR | - | - | + |
MM: meno-metrorrhagia. Echogenicity: anechoic, hypoechoic, isoechoic, hyperechoic, mixed (hypo-hyperechoic). Appearence: homogenous, heterogenous. +: present, -: absent. NR: not to be reached.
Table 2. Statistical Analysis of Case-Based Features.
Age, mean ± SD (min. - max.) | 41.8 ± 9.7 (24 - 52) |
Gravida, mean ± SD (min. - max.) | 5.5 ± 4.4 (0 - 12) |
Parity, mean ± SD (min. - max.) | 3.5 ± 2.2 (0 - 6) |
Menapausal state, n (%) | |
Postmenapause | 1 (16.7) |
Premenapause | 5 (83.3) |
Complaint, n (%) | |
Meno-metrorrhagia | 6 (100) |
Sonography | |
Number of tumor/myoma, mean ± SD (min. - max.) | 1.8 ± 1.6 (1 - 5) |
Margins of the tumor, n (%) | |
Ill-defined | 1 (16.7) |
Well-defined | 5 (83.3) |
Tumor echogenicity, n (%) | |
Hyperechoic | 4 (66.7) |
Mixed | 2 (33.3) |
Tumor heterogenicity, n (%) | |
Heterogenous | 6 (100) |
Cystic appearance, n (%) | |
+ | 2 (33.3) |
- | 4 (66.7) |
Calcification n (%) | |
+ | 3 (50.0) |
- | 3 (50.0) |
Acoustic shadowing, n (%) | |
+ | 4 (66.7) |
- | 2 (33.3) |
Free fluid, n (%) | 0 |
Pathology | |
Procedure, n (%) | |
Myomectomy | 2 (33.3) |
TAH + BSO | 4 (66.7) |
Tumor diameter (cm), mean ± SD (min. - max.) | 9.4 ± 5.6 (3.5 - 20) |
Localization, n (%) | |
Intramural | 5 (83.3) |
Submucous | 1 (16.7) |
Mitosis count (n/10 HPF), mean ± SD (min. - max.) | 8.0 ± 4.7 (4 - 17) |
Atypia, n (%) | |
Mild | 2 (33.3) |
Moderate | 4 (66.7) |
Necrosis, n (%) | |
+ | 2 (33.3) |
- | 4 (66.7) |
Final situation n (%) | |
Recurrence | 1 (20) |
Disease-free | 4 (80) |
NR | 1 |
Follow-up (months), mean ± SD (min. - max.) | 63.4 ± 52.1 (11 - 120) |
There was no statistically significant relevance between sonographic findings and atypia, necrosis and mitosis number (P > 0.05). The recurrence was not in relationship with mitosis, degree of atypia and necrosis. We found no relevance between tumor diameter and mitosis, atypia, necrosis and recurrence. In the developing recurrence case, there were two tumors with largest diameter of 8 cm, moderate atypia, 6 mitosis, and no necrosis. Another myomectomy case was similar: one tumor with largest diameter of 7 cm, moderate atypia, 8 mitosis, and no necrosis.
Discussion
STUMP, which is considered a subtype of uterine smooth muscle tumors, is a rare tumor, so the incidance is not well known. Also there is no consensus on histopathological description.
Clinical signs and symptoms are similar with leiomyoma and leiomyosarcoma [2-4]. Those are pelvic pain, anormal uterine bleeding, pelvic mass, and pelvic pressure sensation or combination of them. Mean age is 45 years [2-4]. Most of the patients are premenopausal [4]. In our cases, mean age was 42. Of the patients, 83.3% were premenapausal. All of them had meno-metrorrhagia.
Preoperative STUMP diagnosis or differentiation from leiomyoma-leiomyosarcoma with imaging modalities is not easy. Bonneau et al published the first study about this in 2013 [5]. In this study, they have compared sonography and MRI findings of 85 leiomyoma and 23 malignant mesenchymal tumor (MMT) and STUMP cases, and reported that presence of single tumor, absence of acoustic shadowing and presence of free fluid are associated with MMT/STUMP. We also retrospectively evaluted our sonography images according to their criteria: four of cases had single tumor, there were no acoustic shadowing in two cases, and none of cases had free fluid. Our sonographic findings showed 83.3% well-defined, 66.7% hyperechoic, 100% heterogenous, 66.7% noncystic, 50% calcification and 66.7% acoustic shadowing.
Uterine smooth muscle tumors have historically been distinct in benign leiomyomas and malignant leiomyosarcomas on the basis of cytological atypia, mitotic rate and presence or absence of tumor cell necrosis (CTCN) [6]. The Stanford criteria for the histologic diagnosis of leiomyosarcoma reported by Bell et al include at least two of the following criteria: diffuse moderate-to-severe atypia, a mitotic count of at least 10 mitotic figures/10 HPF and tumor cell necrosis criteria; absence of necrosis and atypia, ≤ 4 mitosis indicating benign leiomyoma. There is no consensus on diagnostic criteria of STUMP in literature. WHO classification indicates that a uterine SMT not diagnosed unequivocally as benign or malignant should be defined as STUMP. The STUMP tumors were subdivided by Bell et al [6] into three groups: 1) atypical leiomyoma with low risk of recurrence - diffuse moderate-to-severe atypia, < 10 mitosis/10 HPF and no CTCN; 2) atypical leiomyoma but limited experience-severe atypia, < 20 mitosis/10 HPF, no CTCN; and 3) smooth muscle tumor of low malignant potential has CTCN, mitosis less than 10/10 HPF, absent to mild nuclear atypia. Guntupalli et al [2] had diagnosis of STUMP in one of the following criteria: tumor necrosis (+), no atypia, mitosis ≤ 10/10 HPF; diffuse atypia (+), no tumor necrosis, mitosis ≤ 10/10 HPF; no tumor necrosis, no atypia, mitosis ≥ 20/10 HPF; cellularity or hypercellularity with mitosis ≥ 4/10 HPF; irregular margins or vascular invasion in peripheral side of tumor.
D’Angelo and Prat [7] described the following criteria for STUMP: tumor necrosis in typical leiomyoa; necrosis and ≥ 10 mitosis/10 HPF or remarkable diffuse atypia; remarkable diffuse or focal atypia and borderline mitosis; and hardly classified necrosis. Generally, STUMP diagnosis is decided after myomectomy or hysterectomy according to three histological criteria of the Stanford. If the tumor does not meet criteria for leiomyosarcoma, and has combinations of Stanford’s criteria, STUMP diagnosis is accurate.
Reported recurrence rate for STUMP is 7-27% [8, 9]. Tumor necrosis, degree of atypia and mitosis are correlated with malignant behavior, but relationship with recurrence is not clear. Because, the recurrence is observed in single or variable combinations and degrees of those [2-4, 8-12]. Therefore, it is not so easy to foresee biological behavior, metastatic potential or prognosis of STUMP. Recurrence tumor is either STUMP or leiomyosarcoma, and can occur in uterus, pelvis, retroperitoneum, lung, liver and bone [2, 3, 9-12]. In patients with STUMP, tumor growth is slower, and recurrence is often delayed for a mean of 51 months after the initial diagnosis. Furthermore, the clinical course is often delayed, with a median survival of 61.5 months [8]. Five years survival is 92-100% [4, 12]. In our study, mean follow-up duration was 63 months, and recurrence rate was 20%. Five patients were still alive, and four of them were disease-free. In our recurrence case, number of mitosis was 6, with moderate atypia and no necrosis. In this case, recurrence has been diagnosed after 11 months as STUMP.
The recurrence ratio after hysterectomy and myomectomy is similar [2]. Recurrence rate after myomectomy is 6.6% [8]. In post-myomectomy STUMP diagnosis can be performed second myomectomy or hysterectomy according to patients condition. The patient’s age, fertility, pathological properties of tumor, number of recurrence, size and location of the tumor should be carefully considered before deciding the procedure. Successful pregnancy rate after myomectomy is 52% [8]. Patients who desire pregnancy should be informed about potential morbidity and mortality of tumor. Treatment options for recurrence in addition to surgery include adjuvant chemotherapy, radiotherapy, and progestins GnRH analogs [2-4, 8-11]. Our recurrence case was unmarried, 24 years old, and had multiple nodules with the biggest one being 12 cm, and we recommended surgery and adjuvant therapy after detailed briefing.
The patients should undergo baseline assessment and regular follow-up every 6 months for the first 5 years, then annual surveillance for the next 5 years [8]. Follow-up visits should consist of a history, general and pelvic examination, and imaging studies annually including chest radiography, pelvic ultrasound, MRI and/or PET-CT, to detect recurrences.
Conclusion
STUMP is a rare heterogenous tumor. All of the cases were operated with benign preoperative gynecological diagnosis and final diagnosis has been made histopathologically. It is not easy to foresee the biological behavior pattern and prognosis of STUMP. It is classified as an intermediate form histopathologically, so calling it benign or malignant for sure is not possible. We have limited literature information for STUMP. The final histopathological diagnosis is usually made according to Stanford criteria. Preoperatively, sonographic discrimination from leiomyoma or leiomyosarcoma is not possible definitely. Although our case number is limited, singulary, solidity, hyperechogenicity, heterogenocity and features of acoustic shadowing and margins can guide us to preoperative sonographic diagnosis. STUMP is clinically benign, but recurrence/metastasis after many years from operation can be seen, and those patients should be followed long term.
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