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1.
J Indian Assoc Pediatr Surg ; 28(2): 170-172, 2023.
Article in English | MEDLINE | ID: mdl-37197234

ABSTRACT

Historically it was recommended for emergency thoracotomy in thoracic trauma as the last resort when there was cardiopulmonary arrest. Nowadays, the only indications are lung transplantation and huge mediastinal masses. We report the use of a clamshell thoracotomy in a 7-month-old boy with a large anterior mediastinal mass extending into the bilateral thoracic cavities.

2.
J Pediatr Surg ; 58(9): 1843-1848, 2023 Sep.
Article in English | MEDLINE | ID: mdl-37024416

ABSTRACT

BACKGROUND: Common salt is a safe, effective and cheap home-made remedy for umbilical granuloma. The aim of this scoping review is to identify and summarize the available evidence and examine the research conducted on salt treatment for umbilical granuloma. METHODS: A literature search was performed in the second week of September, 2022 using Google scholar, PubMed, MEDLINE and EMBASE databases using the keywords 'umbilical granuloma' and 'salt treatment' to identify all English articles pertaining to salt treatment for umbilical granuloma. Tables were made to summarize the methodological characteristics, results and the dosage regimens of salt used by different authors. The Cochrane Collaboration's tool was used for assessing risk of bias in RCTs. The indexing statuses of the journals publishing these studies were also noted. The overall efficacy with the use of common salt was calculated by adding the success rates mentioned in each study. RESULTS: Twenty-four articles (2 systematic reviews, 6 Randomized Controlled Trials, 11 prospective cohort studies, 1 case control study, 3 retrospective case series and 1 case report) were included. An overall 93.91% success rate (1033/1100) was seen with common salt application, without any reports of complications/recurrences. CONCLUSION: Topical application of common salt for umbilical granulomas is simple, effective and inexpensive. This scoping review provides a broader outlook at the existing level of evidence and may help in planning interventional comparative studies, so that recommendations can be formulated. It also highlights a lack of properly designed randomized controlled trials on this topic. LEVEL OF EVIDENCE: I.


Subject(s)
Granuloma , Sodium Chloride , Humans , Infant , Case-Control Studies , Prospective Studies , Retrospective Studies , Granuloma/drug therapy , Granuloma/etiology , Sodium Chloride/therapeutic use
3.
J Indian Assoc Pediatr Surg ; 27(4): 441-447, 2022.
Article in English | MEDLINE | ID: mdl-36238333

ABSTRACT

Background: There is limited information on the impact of cytomegalovirus (CMV) infection on clinical outcomes and operative histopathology in children with biliary atresia (BA). We hypothesized that CMV infection is associated with greater histopathological damage and unfavorable short-term clinical outcomes. Materials and Methods: A prospective single-center study was conducted with effect from January 2011-July 2012 including all infants with BA who underwent surgery. Diagnosis of CMV infection was confirmed by serum immunoglobulin M (IgM) positivity or the presence of CMV-deoxyribonucleic acid (DNA) in the liver tissue. Four short-term outcome variables were observed. The cohort was divided into subgroups on the basis of seropositivity (IgM + or IgM-); the presence of CMV-DNA in the liver (polymerase chain reaction [PCR]+ or PCR-); and composite CMV groups (Group 1 - IgM+, PCR+; Group 2 - IgM+, PCR-; Group 3 -- IgM-, PCR+; and Group 4 - IgM-, PCR-). Outcomes and histopathology were compared in these subgroups. Results: A total of 32 infants with BA were operated at a mean age of 3.5 (range: 1-6) months. Serum IgM+ and PCR+ were observed in 50% and 37.5% of the patients. Unfavorable outcomes showed a significant association with IgM+ and not PCR+. Similarly, outcomes were poor for CMV Groups 1 and 2 at 1-month follow-up. Infants with IgM+ and PCR+ showed a greater degree of histopathological damage in terms of bile duct proliferation and severe bile duct fibrosis, respectively. Conclusion: In the present study, there was a high incidence of serum IgM+ (50%) and PCR+ of biopsy specimens (37.5%) in infants with BA. This CMV-infected subgroup was associated with greater histopathological damage and unfavorable short-term outcomes after surgery.

5.
J Pediatr Surg ; 46(12): 2387-90, 2011 Dec.
Article in English | MEDLINE | ID: mdl-22152888

ABSTRACT

Clear cell sarcoma of the kidney (CCSK) is a rare renal tumor. Only 4 cases of CCSK with vascular thrombus have been reported, and 2 of these were pediatric cases. One of the children had an intraatrial thrombus as well. We describe a 3-year-old boy who was diagnosed as having a Wilms tumor but did not respond to preresection chemotherapy. He underwent complete resection of the tumor under cardiopulmonary bypass. Histologic examination indicated that the tumor was a CCSK. The patient was then managed with appropriate chemotherapy and radiation therapy and is well 16 months after diagnosis.


Subject(s)
Diagnostic Errors , Heart Atria/pathology , Kidney Neoplasms/diagnosis , Nephrectomy/methods , Sarcoma, Clear Cell/diagnosis , Thrombectomy , Vena Cava, Inferior/pathology , Venous Thrombosis/etiology , Antineoplastic Combined Chemotherapy Protocols/administration & dosage , Antineoplastic Combined Chemotherapy Protocols/therapeutic use , Cardiopulmonary Bypass , Child, Preschool , Combined Modality Therapy , Cyclophosphamide/administration & dosage , Dactinomycin/administration & dosage , Doxorubicin/administration & dosage , Etoposide/administration & dosage , Heart Atria/diagnostic imaging , Heart Atria/surgery , Hepatic Veins/diagnostic imaging , Hepatic Veins/pathology , Hepatic Veins/surgery , Humans , Kidney Neoplasms/complications , Kidney Neoplasms/drug therapy , Kidney Neoplasms/pathology , Kidney Neoplasms/radiotherapy , Kidney Neoplasms/surgery , Male , Neoadjuvant Therapy , Sarcoma, Clear Cell/complications , Sarcoma, Clear Cell/drug therapy , Sarcoma, Clear Cell/pathology , Sarcoma, Clear Cell/radiotherapy , Sarcoma, Clear Cell/surgery , Tomography, X-Ray Computed , Ultrasonography , Vena Cava, Inferior/diagnostic imaging , Vena Cava, Inferior/surgery , Venous Thrombosis/diagnostic imaging , Venous Thrombosis/surgery , Vincristine/administration & dosage , Wilms Tumor/diagnosis
6.
J Pediatr Surg ; 46(6): 1271-3, 2011 Jun.
Article in English | MEDLINE | ID: mdl-21683236

ABSTRACT

Yolk sac tumor (YST) is a germ cell neoplasm usually arising from the gonads. Extragonadal YST has been reported in the mediastinum, retroperitoneum, liver, and pelvis. Primary YST of the common bile duct (CBD) has not been previously reported. We describe an 11-month-old girl with a YST arising from the CBD who presented with obstructive jaundice. Imaging studies revealed an intraluminal CBD mass with intrahepatic biliary dilatation and extraluminal infiltration of the head of the pancreas. A complete resection was carried out, and postoperative chemotherapy with cisplatin, etoposide and bleomycin was administered.


Subject(s)
Biliary Tract Surgical Procedures/methods , Common Bile Duct Neoplasms/pathology , Endodermal Sinus Tumor/pathology , Anastomosis, Roux-en-Y/methods , Biopsy, Needle , Chemotherapy, Adjuvant , Common Bile Duct Neoplasms/drug therapy , Common Bile Duct Neoplasms/surgery , Endodermal Sinus Tumor/drug therapy , Endodermal Sinus Tumor/surgery , Female , Follow-Up Studies , Humans , Immunohistochemistry , Infant , Jaundice, Obstructive/diagnosis , Jaundice, Obstructive/etiology , Laparotomy/methods , Magnetic Resonance Imaging/methods , Neoplasm Staging , Rare Diseases , Risk Assessment , Treatment Outcome
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