Articles

Dentinogenic Ghost Cell Tumour (DGCT) is a rare, locally invasive, solid neoplastic variant of the Calcifying Odontogenic Cyst (COC). It accounts for 2% to 14% of all COCs. In this present report, we discuss a case of a 30-year-old female patient.

Meningioma, a benign tumor arising from arachnoid cells, rarely affects the middle ear (ME) and can either occur solitarily or as a lateral extension of a CPA meningioma. Though benign, these tumors may lead to symptoms like hearing loss, vertigo, tinnitus, and facial numbness due to cranial nerve involvement.

Voice‑related biomarkers have the attention of clinicians and data scientists because they promise objective, low‑cost insights into laryngeal and systemic health. We aimed to combine contemporary evidence, emphasizing methodological quality, regulatory readiness, and the strategic priorities

Acute neonatal dacryocystitis (AND) is a common ocular emergency in neonates, often associated with dacryocystocele. It typically presents with inflammatory swelling in the medial canthal region and can lead to serious complications if untreated.

A 62-year-old female, a known case of carcinoma tongue on chemotherapy with a longstanding tracheostomy (for the past 2 years), presented following accidental intratracheal breakage of a tracheostomy brush during routine care.

The short- and long-term implications following COVID-19 remain unclear. This case report includes a unique case of COVID-19 which was followed with the development of recurrent, widespread thrombosis.

Heterotopic tissue in the gastrointestinal tract is rare, with pancreatic and gastric heterotopia being the most reported types [1]. Heterotopic respiratory mucosa (HRM), particularly in the rectum, is exceedingly rare, with only three cases documented in the literature [2-4].

Pediatric renal tumors are uncommon, with Wilms tumor (WT) being the most frequently diagnosed. Among its subtypes, Botryoid Wilms tumor (BWT) is a rare variant distinguished by its multilobular architecture.

Hemoglobin C (HbC) is a variant that is formed as a result of missense mutation in the coding region of HBB gene. Co-inheritance of hemoglobin C and Beta thalassemia mutations results in Hb C/ Beta thalassemia, a rare hemoglobinopathy.