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1.
N Am J Med Sci ; 5(2): 113-8, 2013 Feb.
Article in English | MEDLINE | ID: mdl-23641372

ABSTRACT

BACKGROUND: Children with adenoid hypertrophy have been shown to harbor pathogenic bacteria in the nasopharynx despite antibiotics. Removal of the adenoid is associated with a reduction in the bacterial count. AIMS: The study was done to determine the bacteriology of the adenoid tissue in chronic adenotonsillitis and adenoid hypertrophy, and determine the antibiotic sensitivity of potential pathogens. MATERIALS AND METHODS: This is a descriptive study conducted on 100 patients aged between three and twelve years who underwent adenotonsillectomy/adenoidectomy. After adenoidectomy, the specimen along with the swab taken from the surface of the adenoid was sent for microbiological examination. After 48 and 96 hours, the microbial growth was identified and the antibiotic-sensitivity pattern of the isolate was studied. RESULTS: Aerobic organisms grew in 93% of the specimens and anaerobic organisms in 68%, whereas 7% had no growth. The surface was predominated by commensals and the pathogens were mainly found in the core. The predominant pathogens were Staphylococcus aureus, Streptococcus pneumoniae, and Enterococcus species. The organisms were resistant to penicillin but showed sensitivity to co-amoxiclav and ciprofloxacin. Co-amoxiclav and ciprofloxacin should be considered as the first line of medical treatment for adenotonsillar diseases. CONCLUSIONS: Infection is the main cause of adenoid hypertrophy. Amoxicillin with potassium clavulanate and ciprofloxacin should be considered as the drugs of choice for all adenotonsillar diseases. Early and prompt treatment of adenoid hypertrophy with appropriate antibiotics will avoid unnecessary exposure to repeated antimicrobial therapy, thereby maintaining the beneficial effects of the normal adenoid flora.

2.
Ear Nose Throat J ; 92(2): 84-7, 2013 Feb.
Article in English | MEDLINE | ID: mdl-23460217

ABSTRACT

We report a case of recurrent Pindborg tumor (calcifying epithelial odontogenic tumor) of the maxilla. The patient was a 34-year-old woman who had been previously diagnosed with Pindborg tumor and treated with curettage. She was subsequently referred to us for evaluation of nasal obstruction. Examination revealed the presence of a mass lesion in the right nasal cavity and right maxilla, which was identified as a recurrence of her earlier Pindborg tumor. The patient was treated with maxillectomy with orbital preservation. Pindborg tumor is a rare odontogenic tumor; when it does occur, it is more often seen in the mandible than in the maxilla. While this tumor is often treated with curettage alone, the aggressive nature of the recurrence in our patient necessitated radical surgery. We report this case to highlight the need to be suitably aggressive in treating these types of tumors in order to avoid recurrence.


Subject(s)
Maxillary Neoplasms/diagnosis , Neoplasm Recurrence, Local/diagnosis , Odontogenic Tumors/diagnosis , Skin Neoplasms/diagnosis , Adult , Curettage , Female , Follow-Up Studies , Humans , Maxilla/pathology , Maxilla/surgery , Maxillary Neoplasms/surgery , Neoplasm Recurrence, Local/surgery , Odontogenic Tumors/surgery , Reoperation , Skin Neoplasms/surgery , Tomography, X-Ray Computed
3.
Ear Nose Throat J ; 92(1): 34-40, 2013 Jan.
Article in English | MEDLINE | ID: mdl-23354890

ABSTRACT

A 4-year-old boy presented with a painless swelling over the right pinna of 4 months' duration. Histopathologic examination of the excised mass revealed features of pilomatricoma-a rare, benign skin neoplasm arising from hair follicle matrix cells. The unusual location of the lesion over the pinna, despite its frequent occurrence in the head and neck, prompted this article. We discuss the etiology, clinical presentation, and management of pilomatricoma of the auricular region.


Subject(s)
Ear Neoplasms/pathology , Hair Diseases/pathology , Pilomatrixoma/pathology , Skin Neoplasms/pathology , Child, Preschool , Ear Auricle , Humans , Male
4.
Indian J Otolaryngol Head Neck Surg ; 63(Suppl 1): 83-4, 2011 Jul.
Article in English | MEDLINE | ID: mdl-22754848

ABSTRACT

Dysphagia is a common clinical symptom for an ENT surgeon in his clinic, evaluation of which may not be a great challenge. The objective of this article is to report a rare cause of dysphagia which may be difficult to diagnose unless specifically thought of. This is a report of a case of dysphagia secondary to myasthenia gravis seen in a young lady along with tongue fasciculation in an early onset case unlike the ones reported in the literature where the patients are elderly and more often males in the late phase of the disease. At times, dysphagia may be seen secondary to some rare causes and may mislead the doctor. A carefully taken history and methodical clinical examination will avoid unnecessary invasive procedures and delay in the diagnosis.

5.
Am J Otolaryngol ; 30(6): 430-1, 2009.
Article in English | MEDLINE | ID: mdl-19880035

ABSTRACT

INTRODUCTION: Many complications and sequelae after laryngectomy have been described in the literature. Here, we are reporting an unusual, till now, unreported complication after laryngectomy. CASE REPORT: A 51-year-old man who underwent total laryngectomy for stage 3 carcinoma of larynx presented with cough on attempting to shave the beard 4 months after the surgery. The management of this patient along with a brief review of the literature is discussed. CONCLUSION: Cross nerve innervation was thought to be the cause for this complication.


Subject(s)
Facial Muscles/innervation , Facial Nerve/pathology , Laryngeal Neoplasms/surgery , Laryngeal Nerves/pathology , Laryngectomy/adverse effects , Anastomosis, Surgical/adverse effects , Facial Nerve/surgery , Humans , Laryngeal Nerves/surgery , Male , Middle Aged , Postoperative Complications
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