Hamartoma of the base of the tongue

doi:10.15406/joentr.2015.02.00041

Journal of

eISSN: 2379-6359

Otolaryngology-ENT Research

Case Report Volume 2 Issue 5

Hamartoma of the base of the tongue

Sohair Mohammed Elameen

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Department of Otolaryngology, ENT Hospital-Khartoum, Sudan

Correspondence: Sohair Mohammed Elameen, Department of Otolaryngology, ENT Hospital-Khartoum, Sudan, Tel 00971501507910

Received: March 23, 2015 | Published: June 9, 2015

Citation: Elameen SM. Hamartoma of the base of the tongue. J Otolaryngol ENT Res. 2015;2(5):175‒176. DOI: 10.15406/joentr.2015.02.00041

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Abstract

Hamartomas of the tongue are rare. A case of a 17- years old male with hamartoma at the base of the tongue is reported. The diagnosis was confirmed by a histopathological and immunohistochemical examination of the mass after excisional biopsy under general anesthesia. The literature is reviewed and discussed.

Keywords: hamartoma, base of the tongue

Introduction

The term ‘‘hamartoma’’ was first used by Albrecht in 1904.¹ Hamartomas are defined as tumor-like, but primary non-neoplastic malformations or inborn errors of tissue development, characterized by an abnormal mixture of tissues indigenous to a part of the body with an excess of one or more of the cellular components.² It may occur in any organ of the body and are common in the spleen, liver, kidneys, lungs and pancreas. However, hamartomas of the tongue are extremely rare.²

Case report

A 17-years old male presented to the ENT referred clinic on November 2013 with history of progressive dysphagia for solid and change of voice for the last 3years. His symptoms started with dysphagia for solid, gradual in onset progressive in nature, associated with nasal regurge but no odynophagia, weight loss, fever, anorexia or other constitutional symptom, also there was no shortness of breathing but there was change of voice, hot potato in nature. There were no other symptoms associated with cardiopulmonary, genitourinary, musculoskeletal, nervous systems. There was no significant past, family, drug or social history.

On examination

Patient fully conscious, vital signs were normal stable:

Heart rate: 76 beat/minute
Respiratory rate: 12/minute
Blood pressure: 110/70

The indirect laryngoscope revealed a mass extending from the left side of the base of the tongue but the inferior limit is invisible because of its size. It was covered with normal mucosa, the mass completely obscuring the laryngeal inlet view.

No cervical lymph nodes were palpable in the neck. Rest of examination of the ear, nose, and neck, as well as general physical examination, was unremarkable.

Investigation

Hematological examinations were normal

Complete blood count
Renal function test and electrolytes
Bleeding profile

Radiological examination of the neck

A thyroid uptake scan was negative for activity in the mass.
X ray lateral view showed oropharyngeal soft tissue shadow over the epiglottis
CT scan of the neck showed suspicious large lobulated heterogeneous enhancing soft tissue mass

Then the decision of examination under general anesthesia and biopsy was taken (Figure 1 & 2).

Figure 1 Lateral soft tissue neck X-ray showing a sizable opacity (white star) projecting from the oropharynx into the hypopharynx causing significant encroachment upon the airways.

Figure 2 Coronal and sagittal reconstructed MDCT images showing the origin of the mass from the left fauces (white arrow) and its extension into the hypopharynx causing significant narrowing of the airways (red arrow).

Operative findings

Intubation was difficult, so tracheotomy was done for anesthetic purposes. There was a firm pedunculated mass arising from the left side of the base of tongue extending to the hypopharynx. No other masses or ulcerations were seen in the area. The oral mass was found to be capsulated, dissected from the tongue base and excised completely and its base was ligated .macroscopically the mass was multilobular, firm, measuring about 8x5x6 cm. Histopathological examination revealed hamartomatus malformation confirmed by immunohistochemistry.

Patient took orally in the 2nd day of the operation and tracheotomy was closed 2days later. Endoscopic follow up in 6 and 12months revealed no recurrence.

Discussion

This patient is the first case of hamartoma base of the tongue reported in Sudan. Hamartomas composed of vascular tissue, or hemangiomas, are most common in the head and neck, mature cartilage outgrowths have been described in the nasal cavity, larynx, trachea, bronchi, and lungs.³

Lingual hamartoma may occur in isolation or in association with syndromes such as oral-facial digital syndrome⁴ its presentation as isolated anomaly is extremely rare, with only 15 previously reported patients, 13 of whom were children.⁵ This Table 1 shows some patients with lingual hamartoma in the English-written medical journals.⁶

Hamartomas do not clearly represent either neoplastic or inflammatory disorders.⁷ The differential diagnosis of mass in the tongue base include lingual thyroid, thyroglossal cyst, dermoid cyst which ruled out preoperatively in this patient by using the thyroid and CT scan respectively, other differential diagnoses include sarcoma ,rhabdomyoma, granular cell tumor, schwannoma, and neurofibroma, but these would be relatively easy to differentiate microscopically and by immunohistochemical markers.

As a rule, the treatment for hamartoma is complete removal; recurrence caused by incomplete excision has been reported.⁸

Conclusion

Although hamartoma of the base of the tongue is rare it should be considered in the differential diagnosis of the tongue base masses and complete removal is mandatory to prevent the recurrence.

Acknowledgments

I am extremely thankful and indebted to Dr. Omer Elsayed, Dr. Mahmoud Aboganaya for sharing their expertise and our young proactive Dr. Azza for her help with the patient. I want to take this opportunity to express gratitude to Dr. Layla from radiology department and Mr. Saravana in Thumbay hospital for their help and support.