Punit Singh Parihar

Sawai ManSingh Medical College and Hospital

Author Statistics

Papers

Citation

H-Index

i-10 index

Research Trends

Author Order

Document Type

Co-Authors

Priyanka Mittal

Indian Institute of Technology Mandi

Praveen N. Mathur

Sawai ManSingh Medical College and Hospital

Manoj Kumar Gupta

Amity University

Aadil Farooq

University of Cyprus

Pramila Sharma

Gyan Vihar University

Ankit Singh

Chandigarh University

Praveen Mathur

Sawai ManSingh Medical College and Hospital

Gunjan Sharma

Uttarakhand Ayurved University

Arka Chatterjee

University of Arizona

Naresh Pawar

Sawai ManSingh Medical College and Hospital

Cooperative Institutions

Sawai ManSingh Medical College and Hospital

Creative Commons

Rajasthan University of Health Sciences

All India Institute of Medical Sciences Jodhpur

Institute of Medical Sciences

Rabindranath Tagore Medical College

All India Institute of Medical Sciences

Jawaharlal Nehru University

Banaras Hindu University

Indiana University – Purdue University Indianapolis

Author Statistics

Papers

Citation

H-Index

i-10 index

Research Field

Spontaneous Esophageal Perforation in an Infant: A Rare Case

Indian Journal of Otolaryngology and Head & Neck Surgery (2020)

Punit Singh Parihar Pawan Singhal Ankit Singh Amreen Singh Ritu Sehra

Watchful waiting

Perforation

10.1007/s12070-020-01993-9

Cite

Citations (2)

Spontaneous Wilms Tumor Rupture: A Preoperative Clinical Diagnosis

Bulletin of Urooncology (2021)

Rahul Gupta Praveen N. Mathur Vinayak Rengan Gunjan Sharma Punit Singh Parihar

Exploratory laparotomy revealed a large ruptured left renal tumor causing antero-medial displacement and compression of the descending colon as shown in the diagrammatic representation (Figure 1).The tumor had ruptured (eroded) intra-peritoneally through a large, 4 × 4 cm size rent in the descending mesocolon (Figure 2) with tumor fragments, necrotic material and hemorrhagic fluid in the pelvic cavity and Morrison's pouch.Dissection of the tumor from the renal fossa AbstractWe report a rare case of a spontaneous Wilms tumor rupture in a 13-month-old male who presented with a rapidly increasing abdominal distension.The child had acute exacerbation of symptoms which precipitated an emergency left radical nephrectomy and renal venectomy (due to densely adherent tumoral embolus in left renal vein and Inferior Vena Cava) indicated for intraperitoneal tumor rupture.Postoperative histopathology confirmed a Wilms tumor; classified as stage IIIc.He is on a three-drug chemotherapy and doing well on follow-up.Preoperative spontaneous Wilms tumor rupture is a clinico-radiological challenge.A high index of suspicion is a prerequisite for diagnosis.However, an upfront emergency radical nephrectomy should be discussed.

10.4274/uob.galenos.2021.2021.6.1

Cite

Citations (0)

Clinical presentation, diagnostic variability and management of intra-abdominal cystic masses in paediatric age group - single institution observational study

International journal of scientific research (2021)

Punit Singh Parihar Pramila Sharma Manoj Kumar Gupta Pradeep Gupta Arvind Shukla

Presentation (obstetrics)

Institution

Source

Cite

Citations (0)

Spachelated Intussusception a Forgotten Entity

Journal of Indian Association of Pediatric Surgeons (2022)

Praveen N. Mathur Priyanka Mittal Punit Singh Parihar Rahul Gupta

Intussusception of one or another type is frequently seen in children and is the most common cause of acute bowel obstruction. This pathology is usually promptly recognized and treated accordingly. But if untreated, this entity can have either of the two outcomes. The first one is death from peritonitis and resulting toxemia, which is the most common one. The second one is spontaneous elimination followed by auto-anastomosis and is extremely infrequent. We report one such case of this rare progression who was found to have old healed small bowel intussusception with luminal narrowing on exploration for acute bowel obstruction. We have also reviewed the world literature to understand the mechanism and circumstances under which this progression occurs.

10.4103/jiaps.jiaps_123_21

Cite

Citations (0)

The Aicardi syndrome.

PubMed (1991)

Vinita Puri Bindiya Gupta Punit Singh Parihar Ishani Anand

Source

Cite

Citations (1)

ENDOSCOPIC THIRD VENTRICULOSTOMY (ETV) IS A BETTER ALTERNATIVE FOR VP SHUNT FAILURE IN NON-COMMUNICATING HYDROCEPHALUS

Indian Journal Of Applied Research (2021)

Ramesh Tanger Dinesh Kumar Barolia Arka Chatterjee Punit Singh Parihar Arun Gupta

CONTEXT: VP Shunt is most commonly used procedure for hydrocephalus but shunt failure is also the common complication in many patients. Endoscopic third ventriculostomy (ETV) is an accepted procedure for the treatment of obstructive hydrocephalus. The aim of our study is to evaluate the success rate AIM AND OBJECTIVE - of ETV in patients of obstructive hydrocephalus formerly treated by ventriculo-peritoneal (VP shunt) shunt. The failure VP shunt was removed before ETV. MATERIALS AND METHOD: This study was conducted between June 2015 and December 2019 in single unit of our department. Twenty one (n=21) patients were enrolled for this study. All patients were admitted with failure of VP shunt. They were known case of non-communicating hydrocephalus previously operated for VP shunt. Six patients were excluded for ETV because CT/MRI show grossly distorted anatomy of ventricles. Endoscopic third ventriculostomy was attempted in 15 patients, but ventriculostomy was done successfully in 10 patients, rests were treated with revision of VP shunt. All patients in this study were radiologically diagnosed RESULTS: case of hydrocephalus due to aqueduct stenosis. They were experienced VP shunt insertion but there were failure of shunt due to any reason. ETV procedures were done successfully in 10 patients. Out of 10 patients one patient needed shunt insertion due ineffective ETV. Shunt revision was done in 11 patients. There was no serious complication during and after ETV procedures. The follow-up period of patients with successful ETV was 6–60 months. This follow-up was uneventful and peaceful for their parents. ETV can be considered as an alternative treatment for the patients w CONCLUSION: ith VP shunt failure with an acceptable success rate of 80%, although long-term follow-up is needed for these patients.

Endoscopic third ventriculostomy

Ventriculostomy

Aqueductal stenosis

Cerebral aqueduct

Communicating hydrocephalus

10.36106/ijar/9302582

Cite

Citations (0)

Vanishing gastroschisis with jejunal atresia and extreme short bowel syndrome: A case series

Journal of Neonatal Surgery (2021)

Naresh Pawar Pramila Sharma Punit Singh Parihar Manika Boipai

Background: Vanishing gastroschisis may occur due to spontaneous partial or complete closure of anterior abdominal wall defect around the viscera, leading to small bowel ischemia and resultant entry/exit level atresia and extremely short length of the remaining bowel. The prognosis is very poor, even after aggressive surgery, and requires prolonged total parenteral nutrition. Case Series: We report two female neonates, one with closed and another with closing vanishing gastroschisis, associated with jejunal atresia and extreme short bowel syndrome. In both patients, the antenatal scans showed gastroschisis without the evidence of vanishing gastroschisis. In both neonates, palliative surgeries were done. Both patients died after a few days due to short bowel syndrome and sepsis. Conclusion: When antenatally detected gastroschisis presents with closed or closing anterior abdominal wall defect, (vanishing gastroschisis), the parents/caregivers must be counseled about the poor prognosis of this condition. A tailored approach to either palliation or aggressive therapy is essential in this rare condition.

Gastroschisis

Short Bowel Syndrome

Intestinal atresia

Abdominal wall defect

10.47338/jns.v10.932

Cite

Citations (0)