Home About us Editorial board Ahead of print Current issue Search Archives Submit article Instructions Subscribe Contact Us Login 
An Official Publication of the Indian Association of Oral and Maxillofacial Pathologists


 
  Table of Contents    
CASE REPORT  
Year : 2014  |  Volume : 18  |  Issue : 2  |  Page : 308-311
 

Primary leiomyosarcoma of the mandible


1 Department of Oral and Maxillofacial Pathology, Dental School of Shahid Beheshti University of Medical Sciences, Tehran, Iran
2 Department of Oral and Maxillofacial Surgery, Dental School of Shahid Beheshti University of Medical Sciences, Tehran, Iran

Date of Web Publication17-Sep-2014

Correspondence Address:
Sepideh Mokhtari
Department of Oral and Maxillofacial Pathology, Dental School of Shahid Beheshti University of Medical Sciences, Velenjak Street, Tehran
Iran
Login to access the Email id

Source of Support: None, Conflict of Interest: None


DOI: 10.4103/0973-029X.140915

Rights and Permissions

 

   Abstract 

Leiomyosarcoma (LMS) is a malignant soft tissue tumor that exhibits smoothmuscle differentiation. Its occurrence in the oral cavity is exceedingly rare. This article presents a 67-year-old woman with 9-month history of a painful tumoral lesion on the right side of mandible. Tumor was composed of fascicles of spindle-shaped cells with cigar-shaped nuclei and eosinophilic cytoplasm. Immunohistochemistry showed that tumor cells were positive for smooth muscle actin (SMA) and desmin. The findings were consistent with the diagnosis of LMS.


Keywords: Leiomyosarcoma, mandible, oral cavity, soft tissue tumor


How to cite this article:
Moghadam SA, Khodayari A, Mokhtari S. Primary leiomyosarcoma of the mandible. J Oral Maxillofac Pathol 2014;18:308-11

How to cite this URL:
Moghadam SA, Khodayari A, Mokhtari S. Primary leiomyosarcoma of the mandible. J Oral Maxillofac Pathol [serial online] 2014 [cited 2019 Nov 13];18:308-11. Available from: http://www.jomfp.in/text.asp?2014/18/2/308/140915



   Introduction Top


Leiomyosarcoma (LMS) is a malignant smooth muscle tumor, which is usually seen in the uterus and gastrointestinal tract. [1] The proportion of malignancies among smooth muscle tumors of the oral cavity is disproportionately high in comparison with the low ratio of malignant to benign smooth muscle tumors in the female genital tract. [2] The sex incidence is approximately equal and patients of all ages in a range of 10 months to 90-years-old may be affected. [3]

The purpose of this manuscript is to describe a case of primary LMS in the mandible with immunohistochemical staining of tumor cells, which was useful for diagnosis.


   Case report Top


A 67-year-old woman was admitted for evaluation of a painful swelling in the right side of mandible with a 9-month history [Figure 1] and [Figure 2]. On panoramic radiographic examination, a large ill-defined radiolucent lesion extending from condyle to symphysis was seen [Figure 3]. Computed tomography (CT) sections presented a destructive soft tissue lesion involving the posterior region of mandible and ramus [Figure 4]. There was no regional lymphadenopathy and CT scan of abdomen, pelvic sonography and chest X-ray were normal.
Figure 1: Photograph shows massive swelling in the right side of mandible

Click here to view
Figure 2: Photograph shows intraoral view of the swelling in the right side of mandible

Click here to view
Figure 3: Panoramic radiograph shows a large ill-defined radiolucent lesion extending from condyle to symphysis

Click here to view
Figure 4: Computed tomography section presents a destructive soft tissue lesion in the posterior region of mandible and ramus

Click here to view


Based on clinical presentation and radiographic features, a malignant odontogenic tumor-like ameloblastic carcinoma and other odontogenic carcinomas were considered as the first differential diagnoses. Ameloblastic carcinoma is an aggressive tumor with a mean age of 33-years and frequently arises from a previous recurrent ameloblastoma. [4] However, this patient was much older with no previous history of recurrent ameloblastoma.

Primary bone malignancies like as osteosarcoma and chondrosarcoma were the next differential diagnoses. Osteosarcoma of the jaw is an uncommon malignancy and presents as a painful swelling, as in this case. However, the mean age of patients is about 33 years and it is more common in males. In addition, the radiographic feature of osteosarcoma contains radiopaque areas in many cases, but the massive radiolucent lesion in this case did not show any calcification or radiopaque areas. Chondrosarcoma is the other primary bone malignancy that occurs in old patients. Nevertheless, chondrosarcoma is not painful in most patients. [4]

The other malignancy that affects the jaw bones is multiple myeloma. However, it is multicentric in bones and more common in men. Moreover, it is associated with some systemic signs and symptoms.

Central mucoepidermoid carcinoma and primary intraosseous carcinoma are also considered in differential diagnoses. Radiographically, central mucoepidermoid carcinoma usually reveals either a unilocular or multilocular radiolucency with well-defined borders [4] in contrast to the ill-defined borders of this case.

Soft tissue sarcomas such as malignant peripheral nerve sheath tumor (MPNST) and LMS are exceedingly rare in the jaw but they should also be considered. Also, metastatic tumors are a major consideration in patients with previous history of malignancy. Post irradiation sarcoma was also excluded, as the patient had no previous history of irradiation.

Hemimandibulectomy was performed under general anesthesia. Gross examination of the resected specimen was a creamy firm tumoral mass, measuring 8 × 5 × 4 cm, extending from condyle to symphysis [Figure 5]. Microscopic examination revealed a malignant mesenchymal tumor that was composed of spindle cell proliferation forming rough bundles and fascicles with interlacing pattern [Figure 6]. Tumor cells frequently had features of cytologic atypia as pleomorphism, hyperchromatism and scattered mitotic figures (five per 10 high power fields). No tumoral necrosis was observed. Spindle cells had blunt-ended, oval, centrally located nuclei and abundant eosinophilic cytoplasm [Figure 7] and [Figure 8].
Figure 5: Gross appearance of resected specimen reveals a creamy firm tumoral mass

Click here to view
Figure 6: Photomicrograph shows a malignant neoplasm composed of fascicles of spindle cells (H&E stain, ×100)

Click here to view
Figure 7: Photomicrograph shows fascicles of spindle cells with eosinophilic cytoplasm (H&E stain, ×400)

Click here to view
Figure 8: Spindle cells show pleomorphism and hyperchromatism (H&E stain, ×400)

Click here to view


Due to these histopathological features, differential diagnoses of a malignant spindle cell tumor, including spindle cell carcinoma, melanoma, LMS, adult spindle cell rhabdomyosarcoma, myofibroma and MPNST were considered.

Spindle cell carcinoma is a high-grade malignancy arising from superficial epithelial layer. This diagnosis was excluded by the absence of any dysplasia or carcinoma insitu of overlying epithelium. As well, malignant melanoma was excluded, as the tumor was not a mucosal lesion and had an origin within mandible. In addition, myofibroma of the jaw has some distinguished clinical and histopathologic features. It is more common in the first four decades of life and has biphasic appearance in histopathology. Adult rhabdomyosarcoma should also be mentioned, as it is a spindle cell tumor. Nevertheless, it has a more myxoid stroma. As well, MPNST shows fascicles of atypical spindle-shaped cells. However, the nuclei are wavy despite the oval blunt-ended morphology in this case.

Therefore, immunohistochemical analysis for desmin, SMA (smooth muscle actin), S100, myogenin and CK(cytokeratin) was performed. The cytoplasm of tumor cells was positive only for SMA [Figure 9] and desmin [Figure 10]. Negative immunoreactivity for S100 was against the neural origin of tumor cells. Spindle cell carcinoma was also excluded, as CK was not expressed in lesional cells. Also, myogenin negativity of tumor cells was against the diagnosis of rhabdomyosarcoma.
Figure 9: Photomicrograph illustrates considerable SMA expression by neoplastic cells (IHC stain, ×100)

Click here to view
Figure 10: Photomicrograph illustrates considerable desmin expression by neoplastic cells (IHC stain, ×100)

Click here to view


These findings, including the morphology of tumor cells and their nuclei with the results of immunohistochemical studies were consistent with the diagnosis of LMS. Unfortunately, patient died because of myocardial infarction 10 days after surgery.


   Discussion Top


Intraoral LMS is an extremely uncommon neoplasm, with about 80 cases reported in the literature. The intraoral locations of these tumors are as follows: cheek, mandible, gingiva, maxilla, floor of the mouth, tongue, soft and hard palate mucosa. [1] Jaw bones appear to be a site of predilection for oral LMS and approximately 50% of these tumors arise in the jaws, predominantly mandible. [3] Mandibular canal may also be the site of origin in some cases of mandibular involvement. [5] Recently, Rege et al., have reported a case of high-grade primaryLMSin the mandible. [6]

Possibility of a metastatic LMS to the oral cavity from other primary sites should always be considered. [2] Oral LMS tends to metastasize to cervical nodes, lung and liver, unlike the LMS in other soft tissues, which rarely has nodal involvement. [7]

Primary and metastatic LMS of the parotid and submandibular glands has also been reported. [8] Metastatic LMS may originate from several potential primary sites and the lung is the most common target tissue for metastatic deposits. [1] Difficulty in the microscopic diagnosis of LMS, especially in its differentiation from leiomyoma, has been widely recognized. [7] Although histologic features such as atypia, cellularity and necrosis are correlated with malignancy, the number of mitoses per high-power field (HPF) seems to represent the most reliable criterion of malignancy. However, the criteria of malignancy differs according to the anatomic location. [2]

These neoplasms may easily be mistaken for other more common tumors including spindle cell carcinoma, spindle cell myoepithelioma and melanoma. [7] Periodic acid-Schiff (PAS) and Masson trichrome stain can be helpful for diagnosis. Longitudinal striations may be seen with phosphotungstic acid hematoxylin (PTAH) stain. Immunohistochemical analysis usually reveals the presence of desmin, muscle-specific actin and SMA. [1] In addition, P53 expression has been associated with higher recurrence rate and shorter survival. [2]

The prognosis of LMS is usually poor. [9] Wide surgical excision with radical neck dissection for lymph node metastases is the mainstay of treatment. Because it has high rate of recurrence and metastasis, long term regular follow up is necessary. [10]

 
   References Top

1.PinheiroJde J, AlvesSde M Jr, Okuda E, Jorge WA, Jaeger RG, de Araújo NS. Primary leiomyosarcoma of the mandible. A case report. Med Oral Patol Oral Cir Bucal 2007;12:E56-9.  Back to cited text no. 1
    
2.Nikitakis NG, Lopes MA, Bailey JS, Blanchaert RH Jr, Ord RA, Sauk JJ. Oral leiomyosarcoma: Review of the literature and report of two cases with assessment of the prognostic and diagnostic significance of IHC and molecular markers. Oral Oncol 2002;38:201-8.  Back to cited text no. 2
    
3.MendoncaEF, Martins da silva C, MeneghiniAJ, Silva GB, Filho JA, Batista AC. Low grade gingival leiomyosarcoma in a child. J Dent Child (Chic) 2008;75:301-5.  Back to cited text no. 3
    
4.Neville BW, Damm DD, Allen CM, Bouquot JE. Oral and Maxillofacial Pathology. 3 rd ed. Philadelphia, PA: WB Saunders CO; 2009.  Back to cited text no. 4
    
5.Ayad W, Dieckmann J, Freitag P, Wierich W. Leiomyosarcoma of the mandibular canal. Possible differential diagnosis of cystic processes of the mandible.Mund Kiefer Gesichtschir 1998;2:42-3.  Back to cited text no. 5
    
6.Rege IC, Costa NL, Batista AC, da Silva CM, MeneghiniAJ, MendonçaEF. High-grade primary leiomyosarcoma in the mandible: Diagnosis and treatment. Head Neck 2013;35:E44-8.  Back to cited text no. 6
    
7.Dry SM, Jorgensen JL, Fletcher CD. Leiomyosarcoma of the oral cavity: An unusual topographic subset easily mistaken for non mesenchymal tumors. Histopathology 2000;36:210-20.  Back to cited text no. 7
    
8.Ferreira M, Malpica A. Metastatic uterine leiomyosarcoma to the submandibular gland. Ann Diagn Pathol 2009;13:208-11.  Back to cited text no. 8
    
9.LoMuzio L, Favia G, Mignogna MD, Piattelli A, Maiorano E. Primary intraoral leiomyosarcoma of the tongue: An immunohistochemical study and review of the literature. Oral Oncol 2000;36:519-24.  Back to cited text no. 9
    
10.Yadav R, Bharathan S. Leiomyosarcoma of the buccal mucosa: A case report with immunohistochemistry findings. J Oral Sci 2008;50:215-8.  Back to cited text no. 10
    


    Figures

  [Figure 1], [Figure 2], [Figure 3], [Figure 4], [Figure 5], [Figure 6], [Figure 7], [Figure 8], [Figure 9], [Figure 10]



 

Top
Print this article  Email this article
            

    

 
   Search
 
  
    Similar in PUBMED
    Search Pubmed for
    Search in Google Scholar for
  Related articles
    Article in PDF (4,513 KB)
    Citation Manager
    Access Statistics
    Reader Comments
    Email Alert *
    Add to My List *
* Registration required (free)  


    Abstract
   Introduction
   Case report
   Discussion
    References
    Article Figures

 Article Access Statistics
    Viewed932    
    Printed18    
    Emailed0    
    PDF Downloaded161    
    Comments [Add]    

Recommend this journal

Journal of Oral and Maxillofacial Pathology | Published by Wolters Kluwer - Medknow
Online since 15th Aug, 2007