1.Ciliated Foregut Cyst of the Gallbladder: A Rare Entity of Childhood
Balla Lohith Raja SEKHAR ; Nitin James PETERS ; Jitender SINGH ; Shailesh SOLANKI ; Kirti GUPTA ; Ravi Prakash KANOJIA ; Jai Kumar MAHAJAN
Advances in Pediatric Surgery 2025;31(1):31-35
A ciliated foregut cyst is a rare developmental anomaly. It develops from the primitive foregut. It is usually located supra-diaphragmatically. Its localization in the gallbladder is very infrequent and has been sparsely reported. We report a rare case of a ciliated cyst of the gallbladder in an 11-year-old female, who presented with complaints of upper abdominal pain for 2 months. She was suspected to have gallbladder duplication or gallbladder diverticulum on imaging. The histopathology reported this anomaly as a ciliated foregut cyst. The ciliated cyst of the gallbladder is a benign congenital lesion. Abdominal ultrasonogram and computed tomography/magnetic resonance imaging are suggestive of a cystic lesion of the gallbladder. The definitive diagnosis is by histopathological examination. This is a rare clinicopathological condition in the pediatric age group. The recommended treatment is laparoscopic cholecystectomy. The role of conservative management has not been established due to the rarity of the condition.
2.Hirschsprung Disease Associated With Pelvic Neuroblastoma: A Rare Neurocristopathic Association
Sravanthi VUTUKURU ; Nitin J PETERS ; Shailesh SOLANKI ; Amita TREHAN ; Kirti GUPTA ; Monika BAWA
Advances in Pediatric Surgery 2024;30(1):32-37
Hirschsprung disease (HSCR) is a genetic disorder with an incidence of 1:5000, seen in the pediatric age group. The association between HSCR and neuroblastoma (NBL), ends of the neurocristopathy spectrum is rare. Less than 10 cases of this association are reported in the literature and the association between the Phox gene and Sox10 gene in the pathophysiology of these is being studied. We report a one-year-old baby, who presented to us, with chronic constipation on regular enemas and laxative usage. There was a history of delayed passage of meconium. At the time of Duhamel’s pull through a well-defined, bilobed hard presacral mass, was encountered. Excision and coccygectomy were done and the pull was completed. The histopathology showed a well-differentiated NBL. Fludeoxyglucose positron emission tomography scan and the N-Myc amplification were negative and the patient was managed with expectant treatment. She is doing well over a 3-year follow-up with no recurrence and good resolution of bowel functions.
3.Clinical behaviour and outcome in pediatric glioblastoma: current scenario
Aditya Kumar SINGLA ; Renu MADAN ; Kirti GUPTA ; Shikha GOYAL ; Narendra KUMAR ; Sushant Kumar SAHOO ; Deepak K. UPPAL ; Chirag K. AHUJA
Radiation Oncology Journal 2021;39(1):72-77
Pediatric glioblastoma (pGBM) is a rare entity accounting for only approximately 3% of all childhood brain tumors. Treatment guidelines for pGBM have been extrapolated from those in adult glioblastoma. Rarity of pGBM and underrepresentation of pediatric population in major studies precludes from defining the ideal treatment protocol for these patients. Maximum safe resection is performed in most of the cases followed by postoperative radiotherapy in children over 3 years of age. Benefit of temozolomide is unclear in these patients. Here, we present the clinicopathological details and outcome of six pGBM patients treated at our institute in 2018–2019.
4.Clinical behaviour and outcome in pediatric glioblastoma: current scenario
Aditya Kumar SINGLA ; Renu MADAN ; Kirti GUPTA ; Shikha GOYAL ; Narendra KUMAR ; Sushant Kumar SAHOO ; Deepak K. UPPAL ; Chirag K. AHUJA
Radiation Oncology Journal 2021;39(1):72-77
Pediatric glioblastoma (pGBM) is a rare entity accounting for only approximately 3% of all childhood brain tumors. Treatment guidelines for pGBM have been extrapolated from those in adult glioblastoma. Rarity of pGBM and underrepresentation of pediatric population in major studies precludes from defining the ideal treatment protocol for these patients. Maximum safe resection is performed in most of the cases followed by postoperative radiotherapy in children over 3 years of age. Benefit of temozolomide is unclear in these patients. Here, we present the clinicopathological details and outcome of six pGBM patients treated at our institute in 2018–2019.
5.Lateral arthroplasty along with buccal fat pad inter-positioning in the management of Sawhney type III temporomandibular joint ankylosis
Vijay Laxmy MALHOTRA ; Virendra SINGH ; JK Dayashankara RAO ; Sunil YADAV ; Pranav GUPTA ; Radhey SHYAM ; Shruti KIRTI
Journal of the Korean Association of Oral and Maxillofacial Surgeons 2019;45(3):129-134
OBJECTIVES:
The objective of this study was to highlight the role of lateral arthroplasty along with interposition of the buccal fat pad (BFP) in the management of Sawhney type III temporomandibular joint (TMJ) ankylosis.
MATERIALS AND METHODS:
Ten patients with TMJ ankylosis (7 unilateral and 3 bilateral, total of 13 joints) were treated with lateral arthroplasty and BFP interposition. The bony bridge of the ankylotic mass on the lateral aspect was resected, leaving a distance of 1.5 to 2.0 cm from the base of the skull to the neck of the condyle. The condyle was left intact. Coronoidectomy was performed on the ipsilateral side via the same approach in all cases. The inter-incisal opening was measured at that time, and if it was less than 35 mm, contralateral coronoidectomy was performed by using the intra-oral approach. After satisfactory inter-incisal mouth opening (≥35 mm) was achieved, the TMJ surgical site was revisited, and BFP was retrieved and used to cover the lateral aspect of the medially placed condyle.
RESULTS:
With lateral arthroplasty, the medially displaced condyle can be left in-situ to maintain the mandibular ramal height and function and to act as a growth center in children. Interposition of the BFP prevents reformation of the lateral bony bridge that was removed.
CONCLUSION
Lateral arthroplasty along with interpositioning of the BFP is a novel technique for managing Sawhney type III ankylosis that achieves management goals while avoiding complex and advanced reconstructive surgical procedures.
6.Lateral arthroplasty along with buccal fat pad inter-positioning in the management of Sawhney type III temporomandibular joint ankylosis
Vijay Laxmy MALHOTRA ; Virendra SINGH ; JK Dayashankara RAO ; Sunil YADAV ; Pranav GUPTA ; Radhey SHYAM ; Shruti KIRTI
Journal of the Korean Association of Oral and Maxillofacial Surgeons 2019;45(3):129-134
OBJECTIVES: The objective of this study was to highlight the role of lateral arthroplasty along with interposition of the buccal fat pad (BFP) in the management of Sawhney type III temporomandibular joint (TMJ) ankylosis. MATERIALS AND METHODS: Ten patients with TMJ ankylosis (7 unilateral and 3 bilateral, total of 13 joints) were treated with lateral arthroplasty and BFP interposition. The bony bridge of the ankylotic mass on the lateral aspect was resected, leaving a distance of 1.5 to 2.0 cm from the base of the skull to the neck of the condyle. The condyle was left intact. Coronoidectomy was performed on the ipsilateral side via the same approach in all cases. The inter-incisal opening was measured at that time, and if it was less than 35 mm, contralateral coronoidectomy was performed by using the intra-oral approach. After satisfactory inter-incisal mouth opening (≥35 mm) was achieved, the TMJ surgical site was revisited, and BFP was retrieved and used to cover the lateral aspect of the medially placed condyle. RESULTS: With lateral arthroplasty, the medially displaced condyle can be left in-situ to maintain the mandibular ramal height and function and to act as a growth center in children. Interposition of the BFP prevents reformation of the lateral bony bridge that was removed. CONCLUSION: Lateral arthroplasty along with interpositioning of the BFP is a novel technique for managing Sawhney type III ankylosis that achieves management goals while avoiding complex and advanced reconstructive surgical procedures.
Adipose Tissue
;
Ankylosis
;
Arthroplasty
;
Child
;
Humans
;
Mouth
;
Neck
;
Reconstructive Surgical Procedures
;
Skull
;
Temporomandibular Joint
7.Disseminated Microfilaremia Associated with Lung Cyst and Empyema: An Autopsy Report.
Kirti GUPTA ; Uma Nahar SAIKIA ; Prateek BHATIA ; Mandeep GARG ; Ajay WANCHU
The Korean Journal of Parasitology 2009;47(1):49-52
Clinical manifestations of extralymphatic disease caused by filariasis are varied and range from symptoms due to tropical pulmonary eosinophilia to hematuria, proteinuria, splenomegaly, and rarely arthritis. Disseminated microfilaremia in association with loculated lung cyst and empyema is of rare occurrence and to the best of our knowledge has not been documented in the literature so far. We report here a case of disseminated microfilaremia due to Wuchereria bancrofti infection accompanied by a lung cyst and empyema in a 21-year-old Indian man.
Animals
;
Cysts/*parasitology/pathology
;
Elephantiasis, Filarial/*parasitology/pathology
;
Empyema/*parasitology/pathology
;
Fatal Outcome
;
Humans
;
Lung Diseases/*parasitology/pathology
;
Male
;
Wuchereria bancrofti/isolation & purification
;
Young Adult

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