Priyatharsini Pari

Priyatharsini Pari

Sri Lakshmi Narayana Istitute of Medical Sciences, Puducherry, India

Profile ID RP-000-2097 Joined 2023-01-18 3 articles
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Articles(3)

Authors: Priyatharsini Pari, Bharathi U, Pradha Velu, Sowndaravel S

DOI: 10.18231/j.jdpo.2021.069  

Volume6

Issue4

Pages322-324

Abstract

Single umbilical artery (SUA) is a condition where one umbilical artery exists. Normally, the umbilical artery contains two umbilical artery and one umbilical vein. The incidence of SUA varies from 0.2% to 0.8%. We present a case of SUA in a term baby with birth weight of 1.7kg delivered by a 28-year-old mother. SUA is a condition which must be kept in mind during histopathological examination since it helps in improving the neonatal and maternal care.   Keywords: Single Umbilical artery, Umbilical cord, Congenital anomalies

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Authors: Priyatharsini Pari, Bharathi U, Priyadharsini J, Pammy Sinha

DOI: 10.18231/j.achr.2021.014  

Volume6

Issue1

Pages57-59

Abstract

Background: Enterobius vermicularis appendicitis is one of the rare finding in the appendectomy specimens. It is most often an incidental finding and its role in the causation of acute appendicitis is the topic of controversy. Case Report: An Indian 27-year-old male presented with symptoms of acute appendicitis. His physical examination and laboratory investigations point towards the diagnosis of acute appendicitis following which open appendectomy was performed. Histopathological evaluation suggests Enterobius vermicularis appendicitis. Patient was given antihelminthic medications and his post-operative course was uneventful. Conclusion: All appendectomy specimens must be searched for the parasite since it has varied histopathological spectrum, and its presence helps in the initiation of appropriate medications. Keywords: Enterobius vermicularis, Appendicitis, Pinworm, Diagnosis.

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Authors: Priyadharsini J, Partho Protim Barman, Priyatharsini Pari

DOI: 10.18231/j.achr.2020.069  

Volume5

Issue4

Pages317-319

Abstract

Background: Angiolymphoid hyperplasia with eosinophilia, a benign vascular tumor is a rare entity. It is characterized by abnormal proliferation of blood vessels with mixed inflammatory infiltrate in the background. Case: We present a case report of Angiolymphoid hyperplasia with eosinophilia in a women of age 47 years. She presented with multiple nodules in the temporal region of scalp. Her IgE levels were normal. Chest X-ray and Skull X-ray was unmarkable and histologically proven to be angiolymphoid hyperplasia with eosinophilia. Result: Multiple nodular lesion in the scalp was diagnosed as Angiolymphoid hyperplasia with eosinophilia. Conclusion: Angiolymphoid hyperplasia with eosinophilia, though a rare entity should be kept in mind for early intervention. Keywords: Angiolymphoid hyperplasia with eosinophilia, Nodule, Vascular neoplasm.

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