S. V. Golhar

Hepatic tumours are relatively rare in children, accounting for 1% - 4% of all paediatric solid tumors, commonest amongst them are hepatoblastoma, neuroblastoma, and vascular tumors (hemangioendothelioma/haemangiomas). Infantile Hepatic hemangioendothelioma (IHHE) is classically characterised by hepatomegaly, jaundice, congestive cardiac failure with high cardiac output, skin haemangiomas, haemolytic anemia, thrombocytopenia(kasabach ‐ Merritt syndrome), normal Alfafeto protein (AFP) levels and hypothyroidism. We report a case of infantile hemangioendothelioma in a 5 day old female neonate with high output cardiac failure, unusually high alpha-fetoproteins, thrombocytosis and polycythaemia, which posed a diagnostic dilemma. Diffuse IHHE is a rapidly growing benign tumor which can lead to poor clinical outcome if not identified early. Serum AFP can’t be relied to exclude IHHE.

Presentation (obstetrics)

Hemangioendothelioma

10.21276/aimdr.2016.2.4.8

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Citations (1)

Congenital vallecular cyst with polydactyly - A rare cause of stridor and failure to thrive.

PubMed (2014)

Khode Nikesh Gosrani S. V. Golhar Jeevan N. Vedi

Congenital vallecular cyst is an uncommon, benign but potentially dangerous condition causing respiratory distress and stridor. It is associated with sudden upper airway obstruction resulting in death due to its anatomical location in neonates and infants. We reported a rare case of 2 months old male infant presented with respiratory obstruction with failure to thrive with polydactyly (rarest finding) and managed timely with appropriate surgical marsupialization.

Failure to Thrive

Marsupialization

Airway obstruction

Polydactyly

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Citations (2)

Association of Squamous Cell Carcinoma of lower lip with Xeroderma Pigmentosa – A Devastating disease

IOSR Journal of Dental and Medical Sciences (2017)

Kanchan Tadke Dr.Vaibhav J. Lahane S. V. Golhar

Xeroderma Pigmentosa is a rare inherited autosomal recessive disease characterised by inability to repair DNA damage caused by UV light.Those affected are extremely sensitive to the UV portion of the light.Affected individuals rapidly develop skin atrophy, splotchy pigmentation, telangectasias and skin cancers.These patients have increased propensity for UV radiation induced mutagenesis.Neoplasms occur commonly in the skin exposed areas.Basal cell carcinomas being the most commonly encountered variety.Squamous cell carcinoma has been infrequently reported.Here we report a case of a 17 year old girl of Xeroderma Pigmentosa with squamous cell carcinoma of lower lip.

10.9790/0853-1601082023

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Citations (4)

Study of intratemporal course of facial nerve and its variations — 25 temporal bones dissection

Indian Journal of Otolaryngology and Head & Neck Surgery (2009)

Rajeshri Kharat S. V. Golhar Chandrakant Patil

Anatomical landmark

Oval window

10.1007/s12070-009-0032-6

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Citations (22)