Open Access

Indolent growth of low-grade myofibroblastic sarcoma of the cheek mimics benign lesions: A case report and literature review

  • Authors:
    • Tessho Maruyama
    • Toshiyuki Nakasone
    • Fumikazu Nimura
    • Akira Matayoshi
    • Toshihiro Kawano
    • Kazuhide Nishihara
    • Akira Arasaki
  • View Affiliations

  • Published online on: April 10, 2017     https://doi.org/10.3892/ol.2017.6020
  • Pages: 4307-4314
  • Copyright: © Maruyama et al. This is an open access article distributed under the terms of Creative Commons Attribution License.

Metrics: Total Views: 0 (Spandidos Publications: | PMC Statistics: )
Total PDF Downloads: 0 (Spandidos Publications: | PMC Statistics: )


Abstract

Low-grade myofibroblastic sarcoma (LGMS) is a neoplasm of the soft tissue characterized by myofibroblastic differentiation. This type of tumor has been observed in various sites in the whole body, but frequently occurs in the head and neck region. It typically presents as a slow‑growing painless mass, which is often mistaken for a benign lesion due to its indolent growth; however, LGMS is a malignant neoplasm. In the present study, a 43‑year‑old female presented with a 14‑mm LGMS lesion in the buccal subcutaneous tissues of the buccinator muscle. The patient had initially noticed the lesion 2‑months prior to presenting at the hospital. Following biopsy, the tumor was surgically resected and no recurrence or metastasis was observed during a follow‑up time of 2 years. To the best of our knowledge, this case is the first report of LGMS located in the buccal subcutaneous tissue of the buccinator muscle. The present study a literature review of 55 cases of this tumor type in the head and neck region was conducted, revealing that the indolent growth of these lesions may contribute to a delay in diagnosis. The average time between the onset of clinical symptoms and hospital admission is 3.9 months, and this form of tumor is frequently misdiagnosed as a benign lesion. Therefore, the present study suggests that an incisional biopsy may be performed to rule out LGMS when clinicians encounter patients with the aforementioned indolent lesions anywhere in the body. In addition, the avoidance of radiotherapy is recommended following resection of the LGMS tumor, as it may induce LGMS recurrence.

Introduction

Low-grade myofibroblastic sarcoma (LGMS) is a neoplasm of the soft tissue characterized by myofibroblastic differentiation, which may occur anywhere in the body but frequently occurs in the head and neck region (1,2). Of those, the most common was the tongue (1). Owing to a previous lack of clear diagnostic criteria, the tumor is considered to more frequently occur than the number of times reflected in the literature (3). Furthermore, reports describing the clinical details such as tumor size, method of treatment, presence or absence of recurrence (local recurrence, regional recurrence and distant metastasis) and patient survival are sparse. Currently, despite being distinctly classified by the World Health Organization (WHO) (3), obtaining a differential diagnosis of this tumor from a benign lesion remains challenging (4). Owing to the scarcity of reported cases, the complete clinical picture of LGMS, including mortality rates, incidence rates, methods of treatment and risk factors, is unclear. Regarding recurrence, Yamada et al (4) reported that tumors larger than 3 cm tended to recur. Metastasis is reportedly rare (3). Therefore, definitive treatment criteria for LGMS remain unknown, and the requirement for postoperative radiotherapy or chemotherapy also remains undetermined. The tumor typically presents as a slow-growing painless mass that is often mistaken for a benign lesion due to its indolent growth; however, it is a malignant neoplasm that is able to recur or metastasize following an extended period of time (1). The present study details a case of a patient with LGMS of the buccal subcutaneous tissues on the buccinator muscle, and reviews 55 relevant cases of head and neck LGMS.

Case report

A 43-year-old Japanese female was referred to University Hospital of the Ryukyus (Okinawa, Japan) in May 2013 by her dentist due to the presence of a mass in the left buccal area that had developed over a 2-month period. The patient had noticed the lesion 2 months earlier, but did not present to the hospital for 2 months. There was no associated pain or paresthesia, and a systematic examination revealed that the patient was otherwise fit and healthy and reported no tobacco or alcohol use (4). The patient's family history indicated that her father had previously been treated for rectal cancer.

A physical examination revealed an elastic hard 13×10 mm mass of the left buccal tissue with distinct margins. The overlying mucosa was normal in color and texture (Fig. 1) and no other causal factors underlying the presence of the mass were observed. The mucosa appeared healthy, no other lesions were observed and no palpable lymphadenopathy was detected in the neck of the patient.

Contrast-enhanced computed tomography (CT) and magnetic resonance imaging (MRI) revealed a 1.4-cm, well-defined mass in the left subcutaneous tissue of the cheek. The lesion was located on the buccinator muscle (Fig. 2, indicated by an arrow), and no other primary or metastatic lesions were detected in all examinations prior to surgery.

A biopsy revealed spindle cell proliferation. Therefore, an excisional biopsy was performed in order to remove the malignant neoplasm. Sections (3 µm) were cut and stained with hematoxylin and eosin. The histopathological results revealed that the tumor was primarily composed of spindle-shaped cells presenting as diffusely infiltrative growth into the surrounding muscle tissues on a myxoid background. The tumor cells were predominately arranged in fascicles, whereas storiform patterns were focally observed. The tumor cells were atypical, with large round or spindle-like nuclei and ill-defined palely eosinophilic cytoplasm. The infiltration of cells around skeletal muscle fibers was also observed (Fig. 3A). Few mitotic cells (<2 mitosis/10 high-power fields; Fig. 3B, indicated by an arrow) were observed and no tumor necrosis was observed (Fig. 3B). The lesions were low grade (5).

Immunohistochemical analysis was performed with the following antibodies: α-smooth muscle actin (1:160; cat. no. M0851; Dako; Agilent Technologies, Inc., Santa Clara, CA, USA); mindbomb E3 ubiquitin protein ligase 1 (MIB-1; 1:100; cat. no. M7240; Dako; Agilent Technologies, Inc.); cluster of differentiation 34 (1:200; cat. no. QB-END/10; Novocastra Laboratories, Newcastle, UK); desmin (1:320; cat. no. M0760; Dako; Agilent Technologies, Inc.); caldesmon (1:100; cat. no. M3557; Dako; Agilent Technologies, Inc.); nuclear β-catenin (1:1,000; cat. no. 610,154; BD Biosciences, San Diego, CA, USA); anaplastic lymphoma kinase (1:50; cat. no. M7195; Dako; Agilent Technologies, Inc.); S-100 protein (1:2,000; cat. no. Z0311; Dako; Agilent Technologies, Inc.); anti-pan cytokeratin antibody 1/3 (1:800; cat. no. M3515; Dako; Agilent Technologies, Inc.); and anti-cytokeratin CAM 5.2 (1:16; cat. no. 349205; BD Biosciences, San Jose, CA, USA). Sections (3 µm) were cut and stained. The results identified that the majority of the spindle cells were focally immunoreactive for α-smooth muscle actin (Fig. 4), and <10% of the lesional cells stained positive for MIB-1 (Fig. 5). By contrast, immunostaining was negative for other markers, including cluster of differentiation 34, desmin, caldesmon, nuclear β-catenin, anaplastic lymphoma kinase, S-100 protein and 2 markers of cytokeratin: anti-pan cytokeratin antibody 1/3 and anti-cytokeratin CAM 5.2. Therefore, the histological and immunohistochemical features of LGMS were diagnosed.

Subsequently, re-excision was performed to obtain clear margins. No residual tumor tissue was observed in the re-excised specimen and no chemotherapy or radiotherapy was administered. At the end of the 2-year follow-up period, the patient was alive and healthy with no clinical or radiological signs of recurrence or metastasis (Fig. 6).

Written informed consent was obtained from the patient for the publication of this case report and all accompanying images. This case report was submitted for ethical review to the Ethics Committee of the University of the Ryukyus (Okinawa, Japan), who waived the requirement for review per institutional protocol, as the study does not contain content that required ethical approval. The Ethics Committee approved the submission and publication of the manuscript.

The first case of LGMS in the head and neck region was described in 1991 (2,6). Literature reports published between 1991 and 2015 were identified using the search terms in PubMed and Google Scholar, excluding non-English language reports. A total of 55 cases were statistically analyzed. Gaussian distribution was confirmed by the Shapiro-Wilk test. Age was evaluated by one-factor analysis of variance (mean ± standard deviation). The size of the tumor was evaluated by the Kruskal-Wallis test (median, minimum-maximum). Recurrence was evaluated by the Fisher's exact test (two-sided). P<0.05 was considered to indicate a statistically significant difference. Analyses were conducted with the use of SPSS for Windows version 22 (IBM SPSS, Armonk, NY, USA).

Discussion

The present study observed 2 important clinical issues. First, to the best of our knowledge, this case is the first report of LGMS in the buccal subcutaneous tissues of the buccinator muscle. Secondly, a literature review of 55 cases of this tumor in the head and neck region revealed that the indolent growth of these lesions may contribute to a delay in the diagnosis of LGMS: the studies reviewed indicated that the average time between the onset of clinical symptoms and hospital admission is 3.9 months.

LGMS has been detected in various sites in the body, including the skin, extremities, trunk, breast, abdominal/pelvic cavity, kidney, vulva, pulmonary artery and bone (2,713), but frequently occurs in the head and neck region (2,14,15). As presented in Table I, LGMS has been reported to occur in a number of locations in the head and neck region (1,2,4,6,13,1540). Of these, three cases of LGMS in the cheek have reported, including the present case, one case located at the nasolabial fold and one from the buccal mucosa (16,23). The most common site was the tongue, followed by the mandible, neck, larynx, palate, maxilla and lips. LGMS was also observed in the gingiva, nasal/paranasal cavity, face, skull, external acoustic meatus, and deep tissue spaces, including the parapharyngeal space, as well as anywhere in the head and neck region (Table I).

Table I.

Cases of LGMS in the head and neck region.

Table I.

Cases of LGMS in the head and neck region.

CaseYearGenderAge, yearsSiteClinical symptoms to admission to the hospital, monthsTumor size, cmTreatmentOutcomeFollow-up, months(Refs.)
  11991M75ParietalNANANALR20(6)
  21991M85FaceNANANANED11(6)
  31992F43Nasolabial21.5Full excisionNANA(16)
  41998F51TongueNA2.5Local excisionNANA(2)
  51998M70TongueNA1.4Local excisionNED42(2)
  61998M24TongueNA1.5Local excisionNED40(2)
  71998M66TongueNA1.8Wide excisionNED28(2)
  81998M19MandibleNA3.5Local excision, RT, CHTNED30(2)
  91999F71Parotid gland41.7Local excisionNED24(17)
102001M41Hard palateNA3.5Wide excisionNED18(15)
112001M35PalateNA1.6Local excisionNED12(15)
122001M63NeckNA4.0NANANA(15)
132001F54GingivaNA1.5Local excisionLR after 4 months4(15)
142001M24Maxillary sinus124.0MaxillectomyNED40(18)
152001F77Nasal cavityNA3.0ExcisionNED14(19)
162001F28NostrilNA1.5Local excisionNANA(20)
172004F  8Pterygoid regionNA6.0Wide excision, CHTNED96(21)
182004F  1Temporal fossa5 weeks2.9Local excisionNED48(21)
192006M42Parapharyngeal space6NART, CHTNED (dead)6(22)
202006F37Buccal mucosa22.0Wide excisionNED6(23)
212006F24Tongue6 weeks2.0Local excisionNED12(24)
222007M41Tongue2 days1.7Local excisionLR after 6 years108(1)
232007F  7NeckNA3.0Surgical resectionNED30(25)
242007M30SkullNA3.0Surgical resectionLR20(25)
252007M32SkullNA4.0Surgical resection, CHTLR46(25)
262007F19External acoustic MeatusNA2.0Surgical resectionNANA(25)
272007M53TongueNA2.0Surgical resection, RTLR28(25)
282007M37NeckNA2.0Surgical resection, RTNED25(25)
292007M44Piriform fossaNA3.0Local excisionLR after 4 years132(26)
302007M74Nasal cavityNA3.0Local resection, RTLR after 9 months27(27)
312007M14Nasal cavityNA5.0Local resection, RTLR after 8 months18(27)
322007M14Ethmoid sinusNA4.5Local resection, RTLR after 9 months32(27)
332007M28Lower lip4 or 52.0Wide local excisionNANA(28)
342009F28Maxillary sinusNA3.0NALR20(13)
352009M52Ethmoid sinusNA6.0NANED13(13)
362009F6.5Maxillary sinusNA3.0NANED24(13)
372009M54Mandible125.9Local excisionNEDNA(29)
382009M51Mandible23.0Local excisionNED24(30)
392009F61Tongue32.0Local excisionNED12(30)
402010M37Mandible gingival32.0Wide excisionNED18(31)
412010M56Tongue baseNA4.2Local excisionNED36(32)
422011F69Larynx616.0Complete excisionNED12(33)
432011F41Laryngeal63.0Wide resectionNED14(34)
442012M73Palate21.0Local excisionNED24(4)
452012M9Mandible13.0Mass excision + alveolectomyNED18(35)
462013M17Upper lip23.4Gross total resectionNED12(36)
472013M44TongueNA2.2Gross total resectionNED2(36)
482013F70NeckNA3.0Unresectable, RT, CHTNED36(36)
492013M55Larynx6NAWide excision, RTNED12(37)
502014M40Larynx3NAWide resectionNED24(38)
512015F75Maxillary sinus1NATotal maxillectomy, RTDM (humerusbone metastasis after 1 year)12(39)
522015M74Tongue baseNA4.1Total laryngectomyLR after 6 months, DT6(39)
532015M45Maxilla65.2MaxillectomyNED30(40)
542015F29MaxillaNA2.5Wide local resectionLR after 6 months12(40)
552015F43Cheek21.4Wide resectionNED18Present case

[i] LGMS, low-grade myofibroblastic sarcoma; M, male; F, female; NA, not applicable; CHT, chemotherapy; RT, radiotherapy; DM, distant metastasis; DT, mortality due to tumor; LR, local recurrence; NED, no evidence of disease.

In addition, the present study demonstrated that the indolent growth of LGMS may contribute to a delay in diagnosis. In the present literature review (Table I), the average time between the onset of clinical symptoms and hospital admission was 3.9 months (the average of this time is presented, with the exception of ‘not applicable’ (NA) cases, in Table I. LGMS is reported as a painless slow growing tumor with a relatively indolent course that mimics a benign lesion (2,4). The majority of patients present with a painless swelling or an enlarged mass (3). These neoplasms arise predominantly in the subcutaneous and deeper soft tissue (3). The present study identified 55 cases of LGMS in the head and neck region published in the English language, including the present case (Table I), with a mean patient age of 42.9 years (median patient age of 42.3 years; range, 1–85) and a male/female ratio of 3:2. Furthermore, the median age at the time of the diagnosis of LGMS in the head and neck region was determined to be younger, compared with that for all head and neck cancer (42.3 years and 60 years, respectively) (41). LGMS lesions are local, aggressive and characterized by frequent recurrence and metastasis, but exhibit a relatively indolent course, and tend to recur locally rather than metastasizing (4,29). However, LGMS is able to metastasize to distant sites, including the left humerus and the cardiac region (39,42). Therefore, disease management via wide excision of the tumor and long-term follow-up is suggested (25). In the present literature review, the rate of local recurrence and distant metastases were 29% (14/49) and 2% (1/49), respectively. In total, 6/55 cases did not provide information regarding the incidence of recurrence or metastasis. None of the 55 studies reviewed reported regional recurrence.

Myofibroblasts were initially identified in 1971 as modified fibroblasts, and are considered to function in the contraction of granulation tissue (43). Myofibroblasts are morphologically and functionally varied, compared with fibroblasts (14), and form the principal component of a number of reactive and benign soft tissue lesions (44). In the past few decades, myofibroblasts have also been identified in malignant soft tissue tumors (6,18). A number of types of sarcoma with predominant myofibroblastic differentiation have been identified and may be categorized into several well-defined clinicopathological entities (26), including LGMS and inflammatory fibroblastic tumor (44). Conversely, non-malignant myofibroblastic lesions include nodular fasciitis and myofibroma (44).

Various studies have provided a detailed analysis of LGMS to date (2,4,13,15,25). The criteria for the classification of LGMS lesions have historically been disputed (45); however, such masses have been distinctly reclassified in the 2013 WHO classification of Soft Tissue and Bone (Fourth Edition) (3). LGMS is sometimes misdiagnosed as a benign lesion (4,31), and a fine-needle aspiration biopsy may be inappropriate because it can obscure the tumor (22,29). Therefore, for the diagnosis of LGMS, incisional biopsy is appropriate (30). An incisional biopsy must be undertaken with caution (27), as if the correct areas are not sampled by the biopsy, including in small or superficial biopsy samples, misdiagnosis may occur owing to the diverse histological appearance of LGMS cells in tissues from the same tumor (27). Until the year 2007, 18 cases of LGMS in the head and neck had been reported (26), whereas by the end of 2015, a total of 55 cases had been identified (Table I), and the case reports of LGMS may continue to increase.

Regarding LGMS treatment, the value of post-operative radiotherapy or chemotherapy remains to be established. Ni et al (34) recommended that the treatment of LGMS include wide excision, with tumor-free margins and post-operative radiotherapy or chemotherapy if required. By contrast, certain reports have described that radiotherapy and chemotherapy are of uncertain clinical value because the tumor was unresponsive. These authors recommended surgical treatment, including excision along the free margin (21,40). Table II presents the recurrence rate (includes metastasis) of the resectable LGMS cases listed in Table I (excluding those with treatments or outcomes indicated as NA) following surgical resection. The recurrence rate following surgery only, as well as following surgery and radiotherapy, was 18.8% (6/32) and 71.4% (5/7), respectively. The statistical analysis revealed that the treatment of surgery and radiotherapy significantly increased the rate of recurrence (P=0.016; Table III). By contrast, the age and the size of tumor showed no bias between the treatments (P=0.312 and 0.162, respectively). According to the aforementioned results, the present study suggests that radiotherapy must be avoided following resection of LGMS, as this treatment may induce the recurrence of LGMS.

Table II.

Recurrence rate and treatment of the LGMS instances reported in Table I.

Table II.

Recurrence rate and treatment of the LGMS instances reported in Table I.

TreatmentNumber of patients (male)Mean age, yearsMean size of tumor, cmNumber of patients with recurrence (rate, %)
Surgery only32 (20)43.4±20.53.16 (18.8)
Surgery + RT7 (6)46±25.43.35 (71.4)
Surgery + CHT2 (1)20±1751 (50)
Surgery + RT + CHT1 (1)193.50 (0)
Total42 (28)42.1±21.53.212 (28.6)

[i] The median size of tumor is calculated, except where NA is stated in Table I. LGMS, low-grade myofibroblastic sarcoma; RT, radiotherapy; CHT, chemotherapy.

Table III.

Comparison of age, tumor size and recurrence between the treatment groups.

Table III.

Comparison of age, tumor size and recurrence between the treatment groups.

Surgery only (n=32)Surgery + RT (n=7)Surgery + CHT (n=2)Surgery + RT + CHT (n=1)P-value
Age (years)43.4±20.546.0±25.420.0±17.019.00.312
Size of tumor (cm)2.9 (1.0–16.0)3.0 (2.0–5.0)5.0 (4.0–6.0)3.5 (3.5–3.5)0.162
Recurrence6 (18.8%)  5 (71.4%)  1 (50.0%)0 (0.0%)   0.016a

a P<0.05 was considered to be statistically significant. Gaussian distribution was confirmed by the Shapiro-Wilk test. Age was evaluated by the one-factor ANOVA (mean ± SD). The size of the tumor was evaluated by the Kruskal-Wallis test (median:minimum-maximum). Recurrence was evaluated by the Fisher's exact test (two-sided). Analyses were conducted with the use of SPSS for Windows version 22 (IBM SPSS, Armonk, NY, USA). RT, radiotherapy; CHT, chemotherapy; SD, standard deviation; n, number of cases.

After a 2-year follow-up period, the patient was alive and healthy with no clinical or radiological evidence of recurrence or metastasis; however, the patient required further observation. In conclusion, to the best of our knowledge, the present case report is the first report of LGMS in the buccal subcutaneous tissue of the buccinator muscle. It is suggested that incisional biopsy be performed to eliminate LGMS when clinicians encounter patients with the aforementioned indolent lesions anywhere in the body. It is also suggested that radiotherapy is avoided following resection of LGMS, as radiotherapy may induce the recurrence of LGMS. Further reports, including long-term follow-up data and adequate clinical information, are required to develop novel treatment protocols for LGMS, and to prevent radiation-induced LGMS, which may be more common than previously considered.

Acknowledgements

The authors would like to thank the staff of the Department of Pathology, University Hospital of the Ryukyus, who contributed to patient diagnosis, and all medical staff at University Hospital of Ryukyus who contributed to the treatment and care of the present patient. In addition, the authors would like to thank Enago (www.enago.jp) for the English language review of the present study.

Glossary

Abbreviations

Abbreviations:

LGMS

low-grade myofibroblastic sarcoma

WHO

World Health Organization

CT

computed tomography

MRI

magnetic resonance imaging

NA

not applicable

RT

radiotherapy

CHT

chemotherapy

References

1 

Jay A, Piper K, Farthing PM, Carter J and Diwakar A: Low-grade myofibroblastic sarcoma of the tongue. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 104:e52–e58. 2007. View Article : Google Scholar : PubMed/NCBI

2 

Mentzel T, Dry S, Katenkamp D and Fletcher CD: Low-grade myofibroblastic sarcoma: Analysis of 18 cases in the spectrum of myofibroblastic tumors. Am J Surg Pathol. 22:1228–1238. 1998. View Article : Google Scholar : PubMed/NCBI

3 

Mentzel T: Low grade myofibroblastic sarcomaWorld Health Organization classification of Soft Tissue and Bone. Fletcher CDM, Bridge JA, Hogendoorn P and Mertens F: 4th. IARC Press; Lyon: pp. 85–86. 2013

4 

Yamada T, Yoshimura T, Kitamura N, Sasabe E, Ohno S and Yamamoto T: Low-grade myofibroblastic sarcoma of the palate. Int J Oral Sci. 4:170–173. 2012. View Article : Google Scholar : PubMed/NCBI

5 

Guillou L, Coindre JM, Bonichon F, Nguyen BB, Terrier P, Collin F, Vilain MO, Mandard AM, Le Doussal V, Leroux A, et al: Comparative study of the national cancer institute and french federation of cancer centers sarcoma group grading systems in a population of 410 adult patients with soft tissue sarcoma. J Clin Oncol. 15:350–362. 1997. View Article : Google Scholar : PubMed/NCBI

6 

Eyden BP, Banerjee SS, Harris M and Mene A: A study of spindle cell sarcomas showing myofibroblastic differentiation. Ultrastruct Pathol. 15:367–378. 1991. View Article : Google Scholar : PubMed/NCBI

7 

Diaz-Cascajo C, Borghi S, Weyers W and Metze D: Fibroblastic/myofibroblastic sarcoma of the skin: A report of five cases. J Cutan Pathol. 30:128–134. 2003. View Article : Google Scholar : PubMed/NCBI

8 

Roth TM, Fratkin J, Woodring TC and McGehee RP: Low-grade myofibroblastic sarcoma of the vulva. Gynecol Oncol. 92:361–364. 2004. View Article : Google Scholar : PubMed/NCBI

9 

Watanabe K, Ogura G, Tajino T, Hoshi N and Suzuki T: Myofibrosarcoma of the bone: A clinicopathologic study. Am J Surg Pathol. 25:1501–1507. 2001. View Article : Google Scholar : PubMed/NCBI

10 

Humphries WE III, Satyan KB, Relyea K, Kim ES, Adesina AM, Chintagumpala M and Jea A: Low-grade myofibroblastic sarcoma of the sacrum. J Neurosurg Pediatr. 6:286–290. 2010. View Article : Google Scholar : PubMed/NCBI

11 

Morgan PB, Chundru S, Hatch SS, Hawkins HK, Adegboyega PA and Eltorky MA: Uncommon malignancies: Case 1. Low-grade myofibroblastic sarcoma of the breast. J Clin Oncol. 23:6249–6251. 2005. View Article : Google Scholar : PubMed/NCBI

12 

Tavora F, Miettinen M, Fanburg-Smith J, Franks TJ and Burke A: Pulmonary artery sarcoma: A histologic and follow-up study with emphasis on a subset of low-grade myofibroblastic sarcomas with a good long-term follow-up. Am J Surg Pathol. 32:1751–1761. 2008. View Article : Google Scholar : PubMed/NCBI

13 

Meng GZ, Zhang HY, Zhang Z, Wei B and Bu H: Myofibroblastic sarcoma vs nodular fasciitis: A comparative study of chromosomal imbalances. Am J Clin Pathol. 131:701–709. 2009. View Article : Google Scholar : PubMed/NCBI

14 

Tomasek JJ, Gabbiani G, Hinz B, Chaponnier C and Brown RA: Myofibroblasts and mechano-regulation ofconnective tissue remodeling. Nat Rev Mol Cell Biol. 3:349–363. 2002. View Article : Google Scholar : PubMed/NCBI

15 

Montgomery E, Goldblum JR and Fisher C: Myofibrosarcoma: A clinicopathologic study. Am J Surg Pathol. 25:219–228. 2001. View Article : Google Scholar : PubMed/NCBI

16 

Eyden BP, Christensen L, Tagore V and Harris M: Myofibrosarcoma of subcutaneous soft tissue of the cheek. J Submicrosc Cytol Pathol. 24:307–313. 1992.PubMed/NCBI

17 

Bisceglia M and Magro G: Low-grade myofibroblastic sarcoma of the salivary gland. Am J Surg Pathol. 23:1435–1436. 1999. View Article : Google Scholar : PubMed/NCBI

18 

Bisceglia M, Tricarico N, Minenna P, Magro G and Pasquinelli G: Myofibrosarcoma of the upper jawbones: A clinicopathologic and ultrastructural study of two cases. Ultrastruct Pathol. 25:385–397. 2001. View Article : Google Scholar : PubMed/NCBI

19 

Kondo S, Yoshizaki T, Minato H, Horikawa I, Tatsumi A and Furukawa M: Myofibrosarcoma of the nasal cavity and paranasal sinus. Histopathology. 39:216–217. 2001. View Article : Google Scholar : PubMed/NCBI

20 

Chang SE, Choi JH, Sung KJ, Moon KC, Koh JK, Lee TJ, Ro JY and Silverman JS: A case of cutaneous low-grade myofibroblastic sarcoma. J Dermatol. 28:383–387. 2001. View Article : Google Scholar : PubMed/NCBI

21 

Keller C, Gibbs CN, Kelly SM, Haller JR, White KS, Coffin CM and Lemons RS: Low-grade myofibrosarcoma of the head and neck: Importance of surgical therapy. J Pediatr Hematol Oncol. 26:119–120. 2004. View Article : Google Scholar : PubMed/NCBI

22 

Takahama A Jr, Nascimento AG, Brum MC, Vargas PA and Lopes MA: Low-grade myofibroblastic sarcoma of the parapharyngeal space. Int J Oral Maxillofac Surg. 35:965–968. 2006. View Article : Google Scholar : PubMed/NCBI

23 

Artopoulou II, Lemon JC, Clayman GL and Chambers MS: Stent fabrication for graft immobilization following wide surgical excision of myofibroblastic sarcoma of the buccal mucosa: A clinical report. J Prosthet Dent. 95:280–285. 2006. View Article : Google Scholar : PubMed/NCBI

24 

Laco J, Simáková E, Slezák R, Tucek L, Mottl R, Spacek J and Ryska A: Low grade myofibroblastic sarcoma of tongue: A case report. Cesk Patol. 42:150–153. 2006.PubMed/NCBI

25 

Meng GZ, Zhang HY, Bu H, Zhang XL, Pang ZG, Ke Q, Liu X and Yang G: Myofibroblastic sarcomas: A clinicopathological study of 20 cases. Chin Med J (Engl). 120:363–369. 2007.PubMed/NCBI

26 

Coyne JD: Low-grade myofibroblastic sarcoma of the piriform fossa: A case report with a literature review of a tumor with a predilection for the head and neck. Br J Oral Maxillofac Surg. 45:335–337. 2007. View Article : Google Scholar : PubMed/NCBI

27 

Meng GZ, Zhang HY, Bu H, Yang GH, Zhang XL and Yang G: Myofibroblastic sarcoma of the nasal cavity and paranasal sinus: A clinicopathologic study of 6 cases and review of the literature. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 104:530–539. 2007. View Article : Google Scholar : PubMed/NCBI

28 

Imanguli MM, Karai LJ, Shanti RM, Stewart DM and Brahim JS: Myofibroblastic tumor of the lower lip in a patient with X-linked hypogammaglobulinemia and isolated growth hormone deficiency: A case report. J Oral Maxillofac Surg. 65:1219–1222. 2007. View Article : Google Scholar : PubMed/NCBI

29 

Niedzielska I, Janic T and Mrowiec B: Low-grade myofibroblastic sarcoma of the mandible: A case report. J Med Case Reports. 10:84582009. View Article : Google Scholar

30 

Demarosi F, Bay A, Moneghini L and Carrassi A: Low-grade myofibroblastic sarcoma of the oral cavity. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 108:248–254. 2009. View Article : Google Scholar : PubMed/NCBI

31 

Montebugnoli L, Venturi M, Gissi DB, Flamminio F and Foschini MP: Low-grade myofibroblastic sarcoma of the gingiva. BMJ Case Rep. 2010:bcr0720103166. 2010. View Article : Google Scholar

32 

Mori T, Shimane T, Hayashi T, Uzuki A, Ikenoya Y, Akiyama R, Egawa S and Sanbe T: Low-grade myofibroblastic sarcoma at the base of the tongue. Showa Univ J Med Sci. 22:239–243. 2010. View Article : Google Scholar

33 

Covello R, Licci S, Pichi B, Spriano G, Vidiri A, Morelli L and Rosenberg AE: Low-grade myofibroblastic sarcoma of the larynx. Int J Surg Pathol. 19:822–826. 2011. View Article : Google Scholar : PubMed/NCBI

34 

Ni C, Xu YY, Zhou SH and Wang SQ: Differential diagnosis of inflammatory myofibroblastic tumor and low-grade myofibroblastic sarcoma: Two case reports with a literature review. J Int Med Res. 39:311–320. 2011. View Article : Google Scholar : PubMed/NCBI

35 

Park KR, Jang HW, Won JH, Kim HS, Cha IH and Kim HJ: Myofibroblastic sarcoma of the mandible: a case report. J Korean Assoc Oral Maxillofac Surg. 38:240–244. 2012. View Article : Google Scholar

36 

Cai C, Dehner LP and El-Mofty SK: In myofibroblastic sarcomas of the head and neck, mitotic activity and necrosis define grade: A case study and literature review. Virchows Arch. 463:827–836. 2013. View Article : Google Scholar : PubMed/NCBI

37 

Khosla D, Yadav BS, Kumar R, Ghoshal S, Vaiphei K, Verma R and Sharma SC: Low-grade myofibroblastic sarcoma of the larynx: A rare entity with review of literature. J Cancer Res Ther. 9:284–286. 2013. View Article : Google Scholar : PubMed/NCBI

38 

Kordač P, Nikolov DH, Smatanová K and Kalfeřt D: Low-grade myofibroblastic Sarcoma of the larynx: Case report and review of literature. Acta Medica (Hradec Kralove). 57:162–164. 2014. View Article : Google Scholar : PubMed/NCBI

39 

Guillermo GO, Ignacio AG, Adriana SAB, Rocío SB, Fátima MP and Modesto AF: Low-grade myofibroblastic sarcoma. Two rare tumors in two rare locations. Rev Esp Cir Oral Maxillofac. 37:108–112. 2015. View Article : Google Scholar

40 

Qiu JY, Liu P, Shi C and Han B: Low-grade myofibroblastic sarcomas of the maxilla. Oncol Lett. 9:619–625. 2015.PubMed/NCBI

41 

Baxi SS, Pinheiro LC, Patil SM, Pfister DG, Oeffinger KC and Elkin EB: Causes of death in long-term survivors of head and neck cancer. Cancer. 120:1507–1513. 2014. View Article : Google Scholar : PubMed/NCBI

42 

Oylumlu M, Yildiz A, Ercan S, Oylumlu M and Davutoglu V: Cardiac metastasis of a low-grade myofibroblastic sarcoma. Echocardiography. 31:E1–E4. 2014. View Article : Google Scholar : PubMed/NCBI

43 

Gabbiani G, Ryan GB and Majne G: Presence of modified fibroblasts in granulation tissue and their possible role in wound contraction. Experientia. 27:549–550. 1971. View Article : Google Scholar : PubMed/NCBI

44 

Fisher C: Myofibroblastic malignancies. Adv Anat Pathol. 11:190–201. 2004. View Article : Google Scholar : PubMed/NCBI

45 

Lagace R, Semir TA, Gabianni G and Schurch W: Myofibroblastic sarcoma. Am J Surg Pathol. 23:1432–1438. 1999. View Article : Google Scholar : PubMed/NCBI

Related Articles

Journal Cover

June-2017
Volume 13 Issue 6

Print ISSN: 1792-1074
Online ISSN:1792-1082

Sign up for eToc alerts

Recommend to Library

Copy and paste a formatted citation
x
Spandidos Publications style
Maruyama T, Nakasone T, Nimura F, Matayoshi A, Kawano T, Nishihara K and Arasaki A: Indolent growth of low-grade myofibroblastic sarcoma of the cheek mimics benign lesions: A case report and literature review. Oncol Lett 13: 4307-4314, 2017.
APA
Maruyama, T., Nakasone, T., Nimura, F., Matayoshi, A., Kawano, T., Nishihara, K., & Arasaki, A. (2017). Indolent growth of low-grade myofibroblastic sarcoma of the cheek mimics benign lesions: A case report and literature review. Oncology Letters, 13, 4307-4314. https://doi.org/10.3892/ol.2017.6020
MLA
Maruyama, T., Nakasone, T., Nimura, F., Matayoshi, A., Kawano, T., Nishihara, K., Arasaki, A."Indolent growth of low-grade myofibroblastic sarcoma of the cheek mimics benign lesions: A case report and literature review". Oncology Letters 13.6 (2017): 4307-4314.
Chicago
Maruyama, T., Nakasone, T., Nimura, F., Matayoshi, A., Kawano, T., Nishihara, K., Arasaki, A."Indolent growth of low-grade myofibroblastic sarcoma of the cheek mimics benign lesions: A case report and literature review". Oncology Letters 13, no. 6 (2017): 4307-4314. https://doi.org/10.3892/ol.2017.6020