12 results on '"Sinha AK"'
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2. Patent Urachus with Patent Vitellointestinal Duct: A Rare Simultaneous Occurrence.
- Author
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Dudhani S, Bachagala K, Suman BK, Rashi R, and Sinha AK
- Abstract
Abstract: A large number of congenital anomalies often involve the umbilicus. This is a report of two such anomalies together in an infant. The child had a mass protruding from the umbilicus since birth. The urachus was noted to be patent on voiding cystourethrogram. On exploration, a patent vitellointestinal duct was also noted. Resection and anastomosis was done for the vitellointestinal duct, and the urachus was excised close to the dome of the bladder. Histopathological examination confirmed a tube lined by intestinal epithelium and the urachal remnant showing a dense fibrous tube-like structure. The omphalo-mesenteric vessels are located between the urachus and the patent vitellointestinal duct, and care should be taken while incising or dissecting in this region to prevent bleeding., (Copyright © 2024 Copyright: © 2024 African Journal of Paediatric Surgery.)
- Published
- 2024
- Full Text
- View/download PDF
3. Female Anorectal Malformation with Genitourinary Prolapse: A Rare Association.
- Author
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Sinha AK, Kumar A, Rashi, Ali MM, and Kumar B
- Subjects
- Humans, Female, Infant, Newborn, Pelvic Organ Prolapse surgery, Pelvic Organ Prolapse diagnosis, Pelvic Organ Prolapse complications, Urogenital Abnormalities surgery, Urogenital Abnormalities complications, Urogenital Abnormalities diagnosis, Colostomy, Anus, Imperforate surgery, Anus, Imperforate diagnosis, Anus, Imperforate complications, Anorectal Malformations surgery, Anorectal Malformations complications, Anorectal Malformations diagnosis
- Abstract
Abstract: Genitourinary prolapse in newborn females as an introital mass is an uncommon entity. The usual causative mechanisms are poor pelvic innervation, damage or pressure on pelvic musculature and ligaments etc. Different methods of reduction as treatment were proposed in the past. Apart from uncommon occurrence of genitourinary prolapse in newborns, its association with anorectal malformation is not reported in English literature after searching on PubMed and Google Scholar. We report three cases of genitourinary prolapse with anorectal malformation in newborn females where decompressing colostomy was curative for the condition reflecting increased intra-abdominal pressure as causative mechanism., (Copyright © 2023 Copyright: © 2023 African Journal of Paediatric Surgery.)
- Published
- 2024
- Full Text
- View/download PDF
4. Gastric Teratoma in Children: A Report of Two Cases and Review of Literature.
- Author
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Ali MM, Raj R, Singh RJ, Rashi R, Kumar A, Sinha AK, and Kumar B
- Subjects
- Humans, Child, Radiography, Teratoma diagnostic imaging, Teratoma surgery
- Abstract
Abstract: Gastric teratomas are very rare tumours. They present with upper abdomen distension which can easily be confused with other common conditions with mass per abdomen in the paediatric age group. Surgical excision is curative for gastric teratomas. The diagnosis is confirmed by radiological evaluation followed by histopathological analysis of excised specimen. We are reporting two such cases of gastric teratomas who presented with complaints of upper abdomen distension. They were evaluated with radiological imaging and successfully managed by surgical excision., (Copyright © 2023 Copyright: © 2023 African Journal of Paediatric Surgery.)
- Published
- 2024
- Full Text
- View/download PDF
5. Inflammatory Myofibroblastic Tumour in Children: A Report of Two Cases and Review of Literature.
- Author
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Sreepriya PP, Ali MM, Rashi R, Kumar A, Sinha AK, Raj S, and Kumar B
- Subjects
- Child, Humans, Neoplasms, Muscle Tissue diagnosis
- Abstract
Abstract: Inflammatory myofibroblastic tumour in paediatric patients present with a diagnostic dilemma because of its clinical, radiological and histopathological features overlapping with other mesenchymal tumours common in this age. Because of its rarity, the exact features are still unclear. Here, we are reporting clinical, radiological and histopathological appearances of two such cases. In both cases, the exact diagnosis was confirmed only after immunohistochemistry. There is a need for further detailed study to exactly determine the natural course and prognosis of these tumours., (Copyright © 2023 Copyright: © 2023 African Journal of Paediatric Surgery.)
- Published
- 2024
- Full Text
- View/download PDF
6. Congenital Urethrocutaneous Fistula.
- Author
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Suman BK, Singh RJ, Sinha AK, and Kumar B
- Subjects
- Male, Humans, Urethra surgery, Hypospadias complications, Hypospadias surgery, Anorectal Malformations complications, Anorectal Malformations diagnosis, Anorectal Malformations surgery
- Abstract
Abstract: Male congenital urethrocutaneous fistula is an extremely rare anomaly that is commonly associated with chordee or anorectal malformations. It is characterised by an abnormal urethral opening on the ventral aspect of the penis with well-formed distal urethra and meatus at the tip of the glans. The treatment is individualised according to the site of the fistula, associated anomalies and condition of the distal urethra. The principles of hypospadias surgery should be strictly followed., (Copyright © 2023 Copyright: © 2023 African Journal of Paediatric Surgery.)
- Published
- 2024
- Full Text
- View/download PDF
7. Giant Colpolithiasis in Urogenital Sinus Anomaly with Urethral Duplication: A Case Report and Review of Literature.
- Author
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Dudhani S, Sinha AK, Kumar B, Kumar A, and Anant M
- Subjects
- Adolescent, Female, Humans, Uterus, Abdominal Wall, Calculi, Urogenital Abnormalities diagnosis, Urogenital Abnormalities diagnostic imaging
- Abstract
Abstract: Primary vaginal calculi are uncommon in children. Urethral duplication in females is seen to occur in association with complex congenital malformations. We report the case of perianal persistent urogenital sinus with a hypertrophied clitoris with phallic urethra, scrotum-like pouch, uterus didelphys with obstructed hemivagina, and giant colpolithiasis in 46XX female. A 16-year-old presented with pain abdomen and cyclic passage of blood clots per rectum. She had a tender lump in left iliac region, a phallus like protrusion and a ruggous sac below it. Vaginal opening was absent. Computed tomography showed two uterine horns with a separate cervix and distended non-communicating hemivaginas with a large calcified oval mass in the left hemivagina. On exploration, calculus was extracted from the left hemivagina. The large calculus found in the left hemivagina appears to be the cause of all presenting symptoms. It obstructed the left hemivagina, filling the left uterine horn with menstrual blood causing its gradual enlargement and secondary infection. The early diagnosis and prompt referral of such an anomaly can only be ensured in institutional deliveries. For a significant proportion of newborns in the developing world, the ability to afford or even be referred to institutes which deal with such cases is a luxurious affair. We hope to bridge bridging the knowledge, attitude and practice gap that exists in our health-care system with this report., (Copyright © 2023 Copyright: © 2023 African Journal of Paediatric Surgery.)
- Published
- 2024
- Full Text
- View/download PDF
8. Advocating for Routine Post-natal Surveillance and Urgent Neonatal Inguinal Hernia Repair.
- Author
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Dudhani S, Jana S, Singh R, Sinha AK, and Kumar B
- Subjects
- Humans, Infant, Newborn, Male, Anastomosis, Surgical, Ileum, Hernia, Inguinal surgery, Intestinal Fistula
- Abstract
Abstract: Inguinal hernias are more common in preterm and neonates and incidence of incarceration are reported to be more in the first 6 months of life. Strangulation follows incarceration and various incarcerated and strangulated contents having been reported in the sac. The fistulation of the herniated content through the scrotal skin is quite rare with only a few reported cases. We present the case of entero-scrotal fistula in a neonate managed with staged repair along with a brief review of the literature. A 27-days-old, full-term male presented with faecal discharge from the right scrotum. He had no tell-tale signs of obstructed hernia. A faecal fistulous opening was located in the right hemi-scrotum. The terminal ileum was seen as the content with an antimesenteric perforation, divided ileostomy and scrotal debridement was done and later ileo-ascending anastomosis was performed electively. Neonatal hernias should be considered an urgency and we advocate early surgery. The resource-limited setting and poor post-natal surveillance may have added to the worries. In our case, swelling and fistulation occurred in a very brief period of 36 h. We managed the child with a diversion stoma followed by ileo-ascending anastomosis later., (Copyright © 2023 Copyright: © 2023 African Journal of Paediatric Surgery.)
- Published
- 2024
- Full Text
- View/download PDF
9. Paediatric laparoscopic inguinal hernia repair: Level of disconnection of peritoneal cuff - An observational study.
- Author
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Ali MM, Rashi R, Sinha AK, Kumar A, and Kumar B
- Subjects
- Male, Female, Child, Humans, Child, Preschool, Pain, Postoperative surgery, Herniorrhaphy methods, Retrospective Studies, Recurrence, Treatment Outcome, Hernia, Inguinal surgery, Laparoscopy methods
- Abstract
Introduction: Inguinal hernia is a common surgical condition in children. Conventionally, the open approach for inguinal hernia repair has been considered the gold standard. However, in the past two decades, laparoscopic inguinal hernia repair has gained popularity among paediatric surgeons as an alternative to the open approach. Apart from good cosmesis and shorter stay at hospital, laparoscopy offers clear-cut advantages of visualising contralateral site and simultaneous repair if it is patent. Many techniques for laparoscopic inguinal hernia repair have been proposed. In this retrospective observational study, we are comparing outcomes between proximal and distal disconnection of hernia sac., Materials and Methods: Ninety-five patients with inguinal hernia were studied in two groups. Group A included 50 patients in which hernia sac was disconnected from the peritoneal cuff proximal to deep inguinal ring (DIR). Group B included 45 patients in which hernia sac was disconnected distal to DIR. Various sociodemographic parameters and intraoperative findings were compared. Outcomes were analysed in terms of post-operative pain, duration of stay at the hospital and recurrences., Results: In group A, there were 46 males and four females with mean age of 4.01 years with standard deviation (SD) of 2.96. Group B included 37 males and eight females with mean age of 5.09 years with SD of 3.56. Excess post-operative pain was observed in 33 patients in Group A with proximal disconnection of hernia sac whereas it was seen in only three patients in Group B with distal disconnection of sac. The P was 0.001 which was highly significant. The duration of stay in the hospital was more in Group A (2.36 ± 1.22 days) as compared to Group B (1.8 ± 0.66 days) with a P of 0.0076 which was significant. Hernia recurrence was seen in four out of 50 patients in Group A (8%) as compared to no recurrence in Group B. However, the difference was not significant., Conclusion: The disconnection of hernia sac distal to DIR is associated with less post-operative pain and shorter duration of hospital stay. There is less recurrence seen in distal disconnection of hernia sac as compared to proximal disconnection; however, to achieve the level of significance, a large cohort study is required., Competing Interests: None
- Published
- 2023
- Full Text
- View/download PDF
10. Giant choledochal cyst in infant: A rare case report.
- Author
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Singh RJ, Ali MM, Rashi R, Kumar A, Dudhani S, and Sinha AK
- Subjects
- Female, Humans, Infant, Liver pathology, Choledochal Cyst diagnosis, Choledochal Cyst diagnostic imaging
- Abstract
The cystic dilatation of the common bile duct (CBD) is a rare pathology in an infant. It is the second-most common surgical cause of cholestatic jaundice in infants after biliary atresia. A 4-month-old female child was admitted to our department with complaints of abdominal distension. The physical examination revealed the presence of a huge palpable mass involving the right hypochondrium up to the right iliac fossa and umbilical region. Ultrasound abdomen revealed a large intra-abdominal cyst but unable to comment on the organ of origin of the cyst due to its huge size. Multidetector computed tomography of the abdomen was suggestive of possible origin of the cyst from CBD extending from porta hepatis to pelvis. At laparotomy, there was a huge choledochal cyst extending from porta hepatis to pelvis. The choledochal cyst was excised, followed by Roux-en-Y hepaticojejunostomy., Competing Interests: None
- Published
- 2023
- Full Text
- View/download PDF
11. Internal fat prolapse from ischiorectal fossa masquerading as currarino syndrome.
- Author
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Ali MM, Kumar A, Rashi R, Sinha AK, and Kumar B
- Subjects
- Anal Canal abnormalities, Anal Canal surgery, Digestive System Abnormalities, Humans, Infant, Male, Prolapse, Rectum abnormalities, Rectum surgery, Sacrum abnormalities, Anorectal Malformations diagnosis, Anorectal Malformations surgery, Syringomyelia
- Abstract
Pelvic magnetic resonance imaging (MRI) is the latest addition to already existing tools for evaluation of anorectal malformation (ARM). It provides detailed information about pelvic floor musculature as well as position of rectal pouch. However, lack of knowledge about normal pelvic floor anatomy can lead to misinterpretation of pelvic MRI which can create confusion and change in approach for surgery. A 14-month-old male child with diagnosis of ARM was evaluated with pelvic MRI. There was finding of abnormal protrusion of fat through the ischiorectal fossa which was misinterpreted as Currarino syndrome which created confusion immediately before posterior sagittal anorectoplasty. Pelvic MRI is highly informative while evaluating a case of ARM. However, a detailed knowledge of pelvic floor anatomy is mandatory to avoid wrong interpretation and misdiagnosis., Competing Interests: None
- Published
- 2022
- Full Text
- View/download PDF
12. Chronic recurrent vomiting associated with primary gastric volvulus in infant: A case report and review of literature.
- Author
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Vaghela MM, Sinha AK, Kumar B, and Kumar P
- Subjects
- Chronic Disease, Female, Humans, Infant, Recurrence, Stomach Volvulus complications, Stomach Volvulus diagnosis, Vomiting etiology, Stomach Volvulus surgery, Vomiting surgery
- Abstract
Gastric volvulus is an uncommon entity found in the paediatric population. We are reporting a case of chronic gastric volvulus presented to us with the complaints of recurrent vomiting after each feed. The vomiting was projectile, nonbilious, and the content was milk. The patient was evaluated by clinical and radiological means in the form of the X-ray abdomen, ultrasound abdomen, upper gastrointestinal (GI) contrast study, and computed tomography scan of the abdomen. The upper GI contrast study was suggestive of gastric volvulus. The patient was operated and gastropexy was done. There was lax gastrocolic ligament with increased distance between stomach and transverse colon without any obvious gastric volvulus. Postsurgery, the patient was symptom-free., Competing Interests: There are no conflicts of interest.
- Published
- 2017
- Full Text
- View/download PDF
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