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Papers by Khalid Khattala

Research paper thumbnail of Transoral Protrusion of a Ventriculoperitoneal Catheter Caused by Jejunal Perforation in an Adult: Rare Case Report and Review of the Literature

World Neurosurgery, 2020

This is a PDF file of an article that has undergone enhancements after acceptance, such as the ad... more This is a PDF file of an article that has undergone enhancements after acceptance, such as the addition of a cover page and metadata, and formatting for readability, but it is not yet the definitive version of record. This version will undergo additional copyediting, typesetting and review before it is published in its final form, but we are providing this version to give early visibility of the article. Please note that, during the production process, errors may be discovered which could affect the content, and all legal disclaimers that apply to the journal pertain.

Research paper thumbnail of La hernie diaphragmatique de Bochdalek étranglée: cause rare d'occlusion intestinale

DOAJ (DOAJ: Directory of Open Access Journals), Mar 1, 2012

ABSTRACT

Research paper thumbnail of The Pre-Diagnosis History of Gynecologic Tumors in Children

Open Journal of Pediatrics

Research paper thumbnail of Pyloric atresia: A rare cause of neonatal gastrointestinal obstruction

Journal of Pediatric Surgery Case Reports

Research paper thumbnail of A congenital epignathus of tongue in a newborn

Journal of Pediatric Surgery Case Reports

Research paper thumbnail of Trans-Mesenteric Hernia in Infants: Report of Two Cases

Journal of Neonatal Surgery

Internal hernias are rare causes of intestinal obstruction in children. Trans-mesenteric hernia r... more Internal hernias are rare causes of intestinal obstruction in children. Trans-mesenteric hernia remains the most common form. We report transmesenteric hernia in a neonate and infant presented with intestinal obstruction.

Research paper thumbnail of Resection of symptomatic focal nodular hyperplasia of the liver with pre-operative angioembolization

Journal of Pediatric Surgery Case Reports

Research paper thumbnail of Urachal cyst abscess associated with a Meckel's diverticulum

Journal of Pediatric Surgery Case Reports

Research paper thumbnail of Rupture of a peritoneal hydatid cyst: Rare cause of acute intestinal obstruction

Journal of Pediatric Surgery Case Reports

Research paper thumbnail of Incarcerated Littre's hernia: A rare complicated form in a little girl

Journal of Pediatric Surgery Case Reports

Research paper thumbnail of Les malformations pulmonaires congénitales: une expérience de 11 ans du service de chirurgie pédiatrique du CHU Hassan II de Fès

Research paper thumbnail of Iconographies supplémentaires de l'article : Une hématidrose et une hémolacrea associées à un trouble de conversion. À propos d’un cas pédiatrique

Elsevier Masson, May 9, 2016

Research paper thumbnail of Iconography : Une hématidrose et une hémolacrea associées à un trouble de conversion. À propos d’un cas pédiatrique

Elsevier Masson, Jun 29, 2016

Research paper thumbnail of Lipoblastoma Located on the Back: A Case of A 7-Month-Old Girl

Journal of Pediatrics & Neonatology, 2021

Introduction: Lipoblastoma is a rare form of a tumor. It is a benign tumor of embryonic adiposis ... more Introduction: Lipoblastoma is a rare form of a tumor. It is a benign tumor of embryonic adiposis tissue that primarily occurs in children younger than 3-years. Lipoblastoma is most located in the extremities and trunk. There is the focal circumscribed lipoblastoma and the infiltrating lipoblastoma. The management is complete surgical resection. Through a clinical description, we report the case of a lipoblastoma in a 7-month-old infant. The study aims to compare the clinical and outcome aspect with those in the literature. Case: A 7-old-month girl, who presents from birth a masse on the right trapezius muscle, fixed 8x 5 cm of large. No inflammatory signs in front of the tumor and no other location. We performed a total resection of the tumor and the pathology analysis found a lipoblastoma. After 2-years of follow-up, there is no recurrent tumor. The patient had no symptoms. Discussion: Lipoblastoma is a rare infant tumor with boy tendency. Another rare localization is reported as t...

Research paper thumbnail of Diagnosis of Peritoneum Tuberculosis during a Herniotomy

Open Journal of Pediatrics, 2020

Background: Tuberculosis is still a public health problem in the third world. The peritoneal loca... more Background: Tuberculosis is still a public health problem in the third world. The peritoneal localization is common even in pediatric patients. The macroscopics aspects of the peritoneal and/or intestine granulations are pathognomonic. However, its diagnosis by an inguinal hernia is exceptional. Our work aims to discuss the particularities of this unusual presentation of peritoneal tuberculosis. Case report: A 10-year-old girl who presented with a painless inguinal hernia. In per operatory, there was a granulomatous inflammation of the vaginalis process. The diagnosis of tuberculosis was confirmed by histopathologic study and the patient started the anti-tuberculosis drugs. After one year of follow-up, the girl is good and has no symptoms. Discussion: Opinions are divided when to cure the hernia. Is it necessary to do a laparoscopic exploration and biopsy then to secondarily cure the hernia; or go through the inguinal way to cure the hernia and do a peritoneal biopsy? In our case, we performed by the same surgical time the cure of the hernia and the biopsy and it did not impact negatively the follow-up. Conclusion: This revelation mode of peritoneal tuberculosis by inguinal hernia is exceptional but possible.

Research paper thumbnail of Uterine Prolapse: The Other Exceptional Complication of Spina Bifida in Newborns

Open Journal of Pediatrics, 2021

Introduction: Spina bifida is the most common neural tube defect. Uterine prolapse is an exceptio... more Introduction: Spina bifida is the most common neural tube defect. Uterine prolapse is an exceptional presentation of its complications. We aim to describe the clinical and progressive features of uterine prolapse in a newborn baby with spina bifida. Observation: 19-day-old newborn. Admitted for spina bifida. The clinical examination showed an anal gaping, the presence of uterovaginal prolapse and bilateral equine varus clubfoot. The particularity was that this prolapse had a spontaneous resolution but appears with screams. We made a compression bandage at the time of resolution. After a 6-month of follow-up, the baby is in good general condition and, there is no recurrence of the prolapse. Conclusion: Uterine prolapse is a rare complication of spina bifida. The main therapeutic component remains the prevention of spina bifida.

Research paper thumbnail of Diagnosis and Surgical Management of Children with Oesophageal Achalasia: A 10-Year Single-Centre Experience in Morocco

African Journal of Paediatric Surgery: AJPS, 2021

Introduction: Achalasia is a primary oesophageal motility disorder with unknown aetiology. The ai... more Introduction: Achalasia is a primary oesophageal motility disorder with unknown aetiology. The aim of this study was to evaluate our 10-year experience in the diagnostic process and surgical management of oesophageal achalasia (OA) in children. Methods: A retrospective review of all children (age: 0–15 years) treated for achalasia at the department of paediatric surgery from 2007 to 2016 was conducted. The demographics, presenting symptoms, associated diseases, diagnostic process, outcomes and complications were analysed. Results: Fourteen patients were identified, with a mean age of 5.2 years. There were eight female and six male patients. The most common symptom was chronic vomiting, in all patients (100%), followed by weight loss in 10 (71.4%), cough in 6 (42.9%), dysphagia in 5 (35.7%) and chest pain in 3 (21.4%). The mean duration of symptoms until diagnosis was 36.3 ± 29.1 months. Three patients underwent an open Heller myotomy (HM) and 11 laparoscopic HM (LHM) including three...

Research paper thumbnail of Kyste hydatique du pancréas révélé par angiocholite chez un enfant

Journal de Pédiatrie et de Puériculture, 2010

Research paper thumbnail of Bilateral maxillo-mandibular syngnathia in a newborn

Pan African Medical Journal, 2014

Research paper thumbnail of Postoperative manic syndrome following removal of a giant cerebral hydatid cyst

Asian Journal of Psychiatry, 2012

Research paper thumbnail of Transoral Protrusion of a Ventriculoperitoneal Catheter Caused by Jejunal Perforation in an Adult: Rare Case Report and Review of the Literature

World Neurosurgery, 2020

This is a PDF file of an article that has undergone enhancements after acceptance, such as the ad... more This is a PDF file of an article that has undergone enhancements after acceptance, such as the addition of a cover page and metadata, and formatting for readability, but it is not yet the definitive version of record. This version will undergo additional copyediting, typesetting and review before it is published in its final form, but we are providing this version to give early visibility of the article. Please note that, during the production process, errors may be discovered which could affect the content, and all legal disclaimers that apply to the journal pertain.

Research paper thumbnail of La hernie diaphragmatique de Bochdalek étranglée: cause rare d'occlusion intestinale

DOAJ (DOAJ: Directory of Open Access Journals), Mar 1, 2012

ABSTRACT

Research paper thumbnail of The Pre-Diagnosis History of Gynecologic Tumors in Children

Open Journal of Pediatrics

Research paper thumbnail of Pyloric atresia: A rare cause of neonatal gastrointestinal obstruction

Journal of Pediatric Surgery Case Reports

Research paper thumbnail of A congenital epignathus of tongue in a newborn

Journal of Pediatric Surgery Case Reports

Research paper thumbnail of Trans-Mesenteric Hernia in Infants: Report of Two Cases

Journal of Neonatal Surgery

Internal hernias are rare causes of intestinal obstruction in children. Trans-mesenteric hernia r... more Internal hernias are rare causes of intestinal obstruction in children. Trans-mesenteric hernia remains the most common form. We report transmesenteric hernia in a neonate and infant presented with intestinal obstruction.

Research paper thumbnail of Resection of symptomatic focal nodular hyperplasia of the liver with pre-operative angioembolization

Journal of Pediatric Surgery Case Reports

Research paper thumbnail of Urachal cyst abscess associated with a Meckel's diverticulum

Journal of Pediatric Surgery Case Reports

Research paper thumbnail of Rupture of a peritoneal hydatid cyst: Rare cause of acute intestinal obstruction

Journal of Pediatric Surgery Case Reports

Research paper thumbnail of Incarcerated Littre's hernia: A rare complicated form in a little girl

Journal of Pediatric Surgery Case Reports

Research paper thumbnail of Les malformations pulmonaires congénitales: une expérience de 11 ans du service de chirurgie pédiatrique du CHU Hassan II de Fès

Research paper thumbnail of Iconographies supplémentaires de l'article : Une hématidrose et une hémolacrea associées à un trouble de conversion. À propos d’un cas pédiatrique

Elsevier Masson, May 9, 2016

Research paper thumbnail of Iconography : Une hématidrose et une hémolacrea associées à un trouble de conversion. À propos d’un cas pédiatrique

Elsevier Masson, Jun 29, 2016

Research paper thumbnail of Lipoblastoma Located on the Back: A Case of A 7-Month-Old Girl

Journal of Pediatrics & Neonatology, 2021

Introduction: Lipoblastoma is a rare form of a tumor. It is a benign tumor of embryonic adiposis ... more Introduction: Lipoblastoma is a rare form of a tumor. It is a benign tumor of embryonic adiposis tissue that primarily occurs in children younger than 3-years. Lipoblastoma is most located in the extremities and trunk. There is the focal circumscribed lipoblastoma and the infiltrating lipoblastoma. The management is complete surgical resection. Through a clinical description, we report the case of a lipoblastoma in a 7-month-old infant. The study aims to compare the clinical and outcome aspect with those in the literature. Case: A 7-old-month girl, who presents from birth a masse on the right trapezius muscle, fixed 8x 5 cm of large. No inflammatory signs in front of the tumor and no other location. We performed a total resection of the tumor and the pathology analysis found a lipoblastoma. After 2-years of follow-up, there is no recurrent tumor. The patient had no symptoms. Discussion: Lipoblastoma is a rare infant tumor with boy tendency. Another rare localization is reported as t...

Research paper thumbnail of Diagnosis of Peritoneum Tuberculosis during a Herniotomy

Open Journal of Pediatrics, 2020

Background: Tuberculosis is still a public health problem in the third world. The peritoneal loca... more Background: Tuberculosis is still a public health problem in the third world. The peritoneal localization is common even in pediatric patients. The macroscopics aspects of the peritoneal and/or intestine granulations are pathognomonic. However, its diagnosis by an inguinal hernia is exceptional. Our work aims to discuss the particularities of this unusual presentation of peritoneal tuberculosis. Case report: A 10-year-old girl who presented with a painless inguinal hernia. In per operatory, there was a granulomatous inflammation of the vaginalis process. The diagnosis of tuberculosis was confirmed by histopathologic study and the patient started the anti-tuberculosis drugs. After one year of follow-up, the girl is good and has no symptoms. Discussion: Opinions are divided when to cure the hernia. Is it necessary to do a laparoscopic exploration and biopsy then to secondarily cure the hernia; or go through the inguinal way to cure the hernia and do a peritoneal biopsy? In our case, we performed by the same surgical time the cure of the hernia and the biopsy and it did not impact negatively the follow-up. Conclusion: This revelation mode of peritoneal tuberculosis by inguinal hernia is exceptional but possible.

Research paper thumbnail of Uterine Prolapse: The Other Exceptional Complication of Spina Bifida in Newborns

Open Journal of Pediatrics, 2021

Introduction: Spina bifida is the most common neural tube defect. Uterine prolapse is an exceptio... more Introduction: Spina bifida is the most common neural tube defect. Uterine prolapse is an exceptional presentation of its complications. We aim to describe the clinical and progressive features of uterine prolapse in a newborn baby with spina bifida. Observation: 19-day-old newborn. Admitted for spina bifida. The clinical examination showed an anal gaping, the presence of uterovaginal prolapse and bilateral equine varus clubfoot. The particularity was that this prolapse had a spontaneous resolution but appears with screams. We made a compression bandage at the time of resolution. After a 6-month of follow-up, the baby is in good general condition and, there is no recurrence of the prolapse. Conclusion: Uterine prolapse is a rare complication of spina bifida. The main therapeutic component remains the prevention of spina bifida.

Research paper thumbnail of Diagnosis and Surgical Management of Children with Oesophageal Achalasia: A 10-Year Single-Centre Experience in Morocco

African Journal of Paediatric Surgery: AJPS, 2021

Introduction: Achalasia is a primary oesophageal motility disorder with unknown aetiology. The ai... more Introduction: Achalasia is a primary oesophageal motility disorder with unknown aetiology. The aim of this study was to evaluate our 10-year experience in the diagnostic process and surgical management of oesophageal achalasia (OA) in children. Methods: A retrospective review of all children (age: 0–15 years) treated for achalasia at the department of paediatric surgery from 2007 to 2016 was conducted. The demographics, presenting symptoms, associated diseases, diagnostic process, outcomes and complications were analysed. Results: Fourteen patients were identified, with a mean age of 5.2 years. There were eight female and six male patients. The most common symptom was chronic vomiting, in all patients (100%), followed by weight loss in 10 (71.4%), cough in 6 (42.9%), dysphagia in 5 (35.7%) and chest pain in 3 (21.4%). The mean duration of symptoms until diagnosis was 36.3 ± 29.1 months. Three patients underwent an open Heller myotomy (HM) and 11 laparoscopic HM (LHM) including three...

Research paper thumbnail of Kyste hydatique du pancréas révélé par angiocholite chez un enfant

Journal de Pédiatrie et de Puériculture, 2010

Research paper thumbnail of Bilateral maxillo-mandibular syngnathia in a newborn

Pan African Medical Journal, 2014

Research paper thumbnail of Postoperative manic syndrome following removal of a giant cerebral hydatid cyst

Asian Journal of Psychiatry, 2012