Managing blood requirement in a rare P-null phenotype patient during the COVID pandemic in a resource-limited setting.

We report the case of a 5-year-old girl with a rare P-null phenotype who presented for a neurosurgical procedure at our center. The case is unique as this patient was one of the two P-null phenotype cases reported in India and we report how we could successfully arrange a rare blood unit for her. As it was challenging to find a donor for her, autologous blood was collected.

Is routine hearing screening necessary in patients with inflammatory bowel disease - a prospective study.

Purpose: To compare audiological profiling and association of hearing loss in different types of IBD and evaluate the degree of hearing impairment based on duration of illness and age parameters.

Methods: 120 subjects evaluated at a tertiary centre were divided into 2 groups- Controls and Cases. Cases were sub grouped into Ulcerative colitis (UC) and Crohn's disease based on biopsy.

A Nose Bleed Reveals Rhabdomyosarcoma's Seed.

Embryonal rhabdomyosarcoma is the malignant mesenchymal proliferation of undifferentiated skeletal muscle. It is the most common soft tissue tumour found in children. Head and neck location accounts for 40% of the cases with the most common variants being of embryonal Nasopharyngeal RMS is a type of parameningeal RMS (arising from tissues adjacent to the meninges) having propensity for CNS and known for having a poorer prognosis, early recurrence, rapid growth and invasion to adjacent structures.

Angiomyxolipoma of the Cheek: A Rare Oral Tumour.

Angiomyxomas, also known as vascular myxolipomas, are a rare type of soft tissue tumor characterized by the proliferation of adipose tissue within a myxoid stroma accompanied by multiple vascular channels. They represent a distinct variant of lipomas and require differentiation from other benign and malignant lipoma subtypes. Despite their rarity, only a few cases of angiomyxolipoma have been documented in medical literature.