1.Mastoid Osteoma: A Case Report
Sethu Thakachy Subha ; Mohamad Doi ; Hemalata Kumari
Malaysian Journal of Medicine and Health Sciences 2016;12(1):71-73
Mastoid osteoma is a rare benign neoplasm of mesenchymal origin. Osteomas of the temporal bone are
infrequent, and these mastoid osteomas are a definite rare occurrence. These tumours can present with
cosmetic deformity and sometimes with pain. In this report we describe a patient with mastoid osteoma
who presented with cosmetic deformity and experienced retro auricular pain.
Osteoma
2.Isolated sphenoid sinusitis: A big headache.
Noor Liza Ishak ; Sethu Thakachy Subha ; Saraiza Abu Bakar
Malaysian Family Physician 2019;14(1):29-30
Isolated sphenoid sinusitis is a rare clinical entity with potentially devastating
complications such as cranial neuropathies, cavernous sinus thrombosis, meningitis and
intracranial abscess. It accounts for only 2.7- 3.0% of all paranasal sinus diseases.1A patient may present with myriad symptoms, ranging from occipital or vertex headache, retro-orbital pain, otalgia, drowsiness to meningitis-like symptoms. With these non-specific and varied symptoms, patients are usually not referred to an otorhinolaryngologist, which contributes to further delay in diagnosis and proper management. Prompt and accurate diagnosis is necessary in order to avoid catastrophic complications due to the proximity of the sphenoid sinus to vital neurovascular structures.
3.Hyalinizing Clear Cell Carcinoma of the Soft Palate - A Case Report
Sharifah Intan Safuraa ; Sethu Subha ; Muhamad Doi ; Sellymiah Adzman
Malaysian Journal of Medicine and Health Sciences 2020;16(No.1):333-4
Hyalinizing clear cell carcinoma presents as a painless submucosal mass commonly located at the palate and base of tongue. It is a rare tumour and has often been misdiagnosed for other more common tumours with clear cytoplasm, such as acinic cell carcinoma, clear cell oncocytoma or mucoepidermoid carcinoma. HCCC has been reported as a low grade malignant tumour with a high rate of cervical metastases. Due to its rarity, there is no treatment protocol. However, the treatment of choice is wide local excision and the neck disease is treated with neck dissection or radiotherapy or both with no conclusive outcome as incidence is too low or underreported with no long term follow up. Our case highlights the diagnosis difficulties in such rare cases, and the need for longer follow up post excision to determine outcome and recurrence rates.