Pleomorphic adenoma of minor salivary gland with therapeutic misadventure: a rare case report
© Thakur et al; licensee BioMed Central Ltd. 2010
Received: 27 August 2009
Accepted: 8 January 2010
Published: 8 January 2010
The benign tumors of nasopharynx are least encountered tumors in otolaryngology, as nasopharynx is considered one of notorious anatomical site for the malignant tumors. Pleomorphic adenoma of the minor salivary gland of nasopharynx and parapharyngeal space is rare. We present a pleomorphic adenoma of minor salivary gland which was mismanaged.
An adult male presented with left nostril obstruction for five months. The examination found big mass extending from nasopharynx to oropharynx. On CT scan, this tumor was quite big and extending to the parapharyngeal space. The FNAB found it a carcinoma but it did not respond to radiotherapy. The excision biopsy of tumor revealed it as pleomorphic adenoma. We found only five published reports on this tumor arising from nasopharynx.
Discussion and conclusion
Although, in this case report exact origin of the tumor could not be ascertained as it also appeared to be a parapharyngeal tumor but we kept the possibility of a nasopharyngeal tumor on the basis of clinical features. The pleomorphic adenoma of nasopharynx is rare. It can be misdiagnosed as malignant epithelial tumor on histopathology. The differentiation from its malignant variant is also difficult. A possibility of benign tumor should always be kept in nasopharyngeal growth with no evidence of metastasis, and histopathological diagnosis of growth should be available before any definitive treatment.
Benign tumors of nasopharynx are rare since nasopharynx is a common site for malignant tumors. Pleomorphic adenoma is the most common benign tumor of the major and minor salivary glands, but rarely found in the nasopharynx. In this case report, we present a case of a large pleomorphic adenoma arising in the nasopharynx and extending to oropharynx that was diagnosed and managed as squamous cell carcinoma.
In Sep 2007, a 35-year-old male presented with a progressive nasal obstruction associated with left aural fullness, hearing loss and hyponasal speech for the past five months. Later, the patient saw a mass pushing the soft palate downwards and began having difficulty in swallowing solid food. On examination, there was a mass behind and above the soft palate, which appeared to be arising from nasopharynx. Neck examination was found normal. Past history included a pyelolithotomy and gastrojujenostomy for duodenal ulcer.
In retrospective review of the CT scans, there could be a possibility of tumor arising in the parapharyngeal space and extending to nasopharynx but clinical progression of the tumor and normal neck examination was in favor of nasopharyngeal origin. Parapharyngeal benign tumors have classical features of sub mucosal swelling in the lateral pharyngeal wall with or without extension to retromandibular area or the submandibular triangle, and bimanually ballot ability. These tumors can have additional features of otalgia, neuralgia, trismus, and paresis/palsies of 9th, 10th or 11th cranial nerves [1, 2].
The fossa of Rosenmuller is a common site of squamous cell carcinoma of the nasopharynx. Nasal obstruction, epistaxis and adenopathy are common symptoms of nasopharyngeal carcinoma; however, the exact diagnosis of nasopharyngeal growth can be made only by an accurate histopathology. The exact site of tumor origin in this case report could be debatable but we present this case because a major mistake occurred by not performing a direct tumor biopsy before starting chemo-radiation.
Palate, nasal cavity and nasopharynx have abundant minor salivary glands and pleomorphic adenoma is the most common benign tumor of these glands. Pleomorphic adenoma arising in the nasal cavity has scanty or absent cartilaginous component which can make histological diagnosis difficult . Compagno and Wong  reported that microscopically pleomorphic adenoma of the nasal cavity resembles mixed tumor of the major salivary glands but due to high epithelial cellularity and little stromal component these benign tumor can be mistaken for malignant epithelial neoplasm. Lam et al.  found skeletal muscle differentiation in pleomorphic adenoma of the nasopharynx which can simulate rhabdomyosarcoma.
Malignant tumors comprise about 40-50% in all the minor salivary gland tumors (7% are carcinoma ex pleomorphic adenoma) [6–9]. Pleomorphic adenoma has three malignant varieties: carcinoma ex pleomorphic adenoma, carcino-sarcoma and metastasizing pleomorphic adenoma. Carcinoma ex pleomorphic adenoma is a rare mixed tumor developing from the epithelial component of the pleomorphic adenoma [9–11]. The malignant transformation in the pleomorphic adenoma has been linked to recurrence and multiple excisions [12, 13], laminin, and collagen IV deposition [14, 15]. Recently , it has been found that loss of β-catenin adhesion molecule is one of the factors responsible for development of pleomorphic adenoma and cytoplasmic accumulation of this molecule causes malignant transformation in pleomorphic adenoma.
CT scan does not provide significant differentiation between carcinoma ex pleomorphic adenoma (CXPA) and benign pleomorphic adenoma as CXPA can have malignant appearance or benign features similar to pleomorphic adenoma. On MRI, low T1 and T2-weighted signal intensity has been suggested as an indicator for carcinoma ex pleomorphic adenoma .
An extensive literature review revealed only five cases of pleomorphic adenoma arising in the nasopharynx [5, 18–21]. Roh et al.  excised a pleomorphic adenoma of nasopharynx in a 61-year-old female by endoscope. They advocated use of endoscope in these cases to avoid injury to eustachian tube. Lee et al.  reported a similar case in an elderly patient who had otalgia, aural fullness and tinnitus. The tumor was excised endoscopically and patient had no recurrence.
The pleomorphic adenoma was undergoing malignant changes or it was a misdiagnosis, we could not ascertain the exact pathology, as we had no pre-radiotherapy histopathological evidence. However, who was at fault: clinician by not following the advice of pathologist for a direct biopsy, or oncologist who started chemo-radiation without any histopathological proof? We cannot blame anyone rather than ourselves as the clinician are the most accountable.
The possibility of benign tumor should be kept in the differential diagnosis of nasopharyngeal tumor without adenopathy.
Clinician should follow pathologist's advice, carefully interpret the cytological diagnosis, and consult the pathologist, whenever in doubt.
An adequate tissue specimen should be obtained especially for cytological diagnosis as pleomorphic adenoma can simulate as a carcinoma.
No patient should be taken for chemo-radiation without any histopathological evidence.
Written informed consent was obtained from the patient for publication of this case report and any accompanying images. A copy of the written consent is available for review by the Editor-in-Chief of this journal.
Financial and Non-Financial Disclosure
List of abbreviations used
- FNAB :
Fine needle aspiration biopsy
- CT :
- MRI :
Magnetic resonance image
- CXPA :
Carcinoma ex pleomorphic adenoma
- H & E :
Hemotoxylin and Eosin
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