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  1. Article ; Online: Mucocele of the tongue.

    Mandhan, Parkash / Napaki, Sarbar / Ali, Mansour

    ANZ journal of surgery

    2015  Volume 87, Issue 12, Page(s) E327–E328

    MeSH term(s) Child, Preschool ; Female ; Humans ; Mucocele/pathology ; Mucocele/surgery ; Tongue Diseases/pathology ; Tongue Diseases/surgery
    Language English
    Publishing date 2015-05-19
    Publishing country Australia
    Document type Case Reports ; Journal Article
    ZDB-ID 2050749-5
    ISSN 1445-2197 ; 1445-1433 ; 0004-8682
    ISSN (online) 1445-2197
    ISSN 1445-1433 ; 0004-8682
    DOI 10.1111/ans.13180
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article: Juvenile colorectal polyps in children: experience in Pakistan.

    Mandhan, Parkash

    Pediatric surgery international

    2004  Volume 20, Issue 5, Page(s) 339–342

    Abstract: Juvenile colorectal polyps are the most common cause of pediatric hematochezia and contribute to significant morbidity if not treated early. This report describes an experience with juvenile colorectal polyps in children (< or =14 years) from Pakistan. ... ...

    Abstract Juvenile colorectal polyps are the most common cause of pediatric hematochezia and contribute to significant morbidity if not treated early. This report describes an experience with juvenile colorectal polyps in children (< or =14 years) from Pakistan. In a 3-year period, 154 polyps were documented in 129 children. The mean age at presentation was 5.2 years, with a male predominance. Most children presented with painless rectal bleeding (+/-13 months) associated with other symptoms, such as protrusion of a mass through the anus, diarrhea, and recurrent abdominal pain. Anemia was observed in 54 children, of whom 14 (26%) required blood transfusion before intervention. Diagnosis was made by digital rectal examination, proctosigmoidoscopy, and barium enema. The average distance of a colorectal polyp was 4 cm from the anal verge. In 108 (84%) children the polyps were solitary, whereas 21 patients had more than one polyp (maximum three) at different locations in the rectosigmoid area. All polyps were successfully removed by proctosigmoidoscopy. Histological examination revealed dysplastic changes in one case, while the rest were inflammatory. Recurrence occurred in seven children within 1 year of initial removal. Juvenile colorectal polyps contribute to a substantial morbidity in children and do carry a minimal risk of developing dysplastic changes, and therefore should be removed early.
    MeSH term(s) Child, Preschool ; Colonic Polyps/complications ; Colonic Polyps/diagnosis ; Colonic Polyps/pathology ; Colonic Polyps/surgery ; Female ; Gastrointestinal Hemorrhage/etiology ; Humans ; Intestinal Polyps/complications ; Intestinal Polyps/diagnosis ; Intestinal Polyps/pathology ; Intestinal Polyps/surgery ; Male ; Pakistan ; Rectal Diseases/complications ; Rectal Diseases/diagnosis ; Rectal Diseases/pathology ; Rectal Diseases/surgery ; Rectum
    Language English
    Publishing date 2004-05
    Publishing country Germany
    Document type Journal Article
    ZDB-ID 632773-4
    ISSN 0179-0358
    ISSN 0179-0358
    DOI 10.1007/s00383-004-1194-7
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Laparoendoscopic removal of peroral extrusion of a ventriculoperitoneal shunt.

    Mandhan, Parkash / Wong, Marilyn / Samarakkody, Udaya

    Asian journal of endoscopic surgery

    2015  Volume 8, Issue 1, Page(s) 95–97

    Abstract: Introduction: Ventriculoperitoneal shunts for hydrocephalic children are known to cause serious complications such as GI perforation. Peroral extrusion of the peritoneal part of a ventriculoperitoneal shunt is very rare, and management could be a ... ...

    Abstract Introduction: Ventriculoperitoneal shunts for hydrocephalic children are known to cause serious complications such as GI perforation. Peroral extrusion of the peritoneal part of a ventriculoperitoneal shunt is very rare, and management could be a challenge.
    Materials and surgical technique: An 11-year-old girl presented with peroral extrusion of the distal end of a ventriculoperitoneal shunt tube. Endoscopy and imaging studies showed that the peritoneal end had perforated the stomach and then extruded from the mouth. We used a surgical technique that combined endoscopy and laparoscopy to manage this rare complication.
    Discussion: Peroral extrusion of a ventriculoperitoneal shunt tube occurs secondary to perforation of the upper GI tract. Managing this condition involves removing the shunt tube, attention to the perforated viscus and associated infection. A combination of endoscopy and laparoscopy provided superior views, enabled identification of the site and size of the perforated viscus, and facilitated the uneventful removal of the tube.
    MeSH term(s) Child ; Device Removal/methods ; Endoscopy, Gastrointestinal/methods ; Female ; Foreign-Body Migration/complications ; Foreign-Body Migration/surgery ; Humans ; Laparoscopy/methods ; Mouth ; Stomach Rupture/complications ; Stomach Rupture/surgery ; Ventriculoperitoneal Shunt/adverse effects
    Language English
    Publishing date 2015-02
    Publishing country Japan
    Document type Case Reports ; Journal Article
    ZDB-ID 2492135-X
    ISSN 1758-5910 ; 1758-5902
    ISSN (online) 1758-5910
    ISSN 1758-5902
    DOI 10.1111/ases.12157
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article: A Triad of Congenital Diaphragmatic Hernia, Meckel's Diverticulum, and Heterotopic Pancreas.

    Mandhan, Parkash / Al Saied, Amer / Ali, Mansour J

    Case reports in pediatrics

    2014  Volume 2014, Page(s) 725945

    Abstract: Congenital diaphragmatic hernia is a common developmental anomaly encountered by paediatric surgeons. It is known to be associated with extradiaphragmatic malformations, which include cardiac, renal, genital, and chromosomal abnormalities. Herein, we ... ...

    Abstract Congenital diaphragmatic hernia is a common developmental anomaly encountered by paediatric surgeons. It is known to be associated with extradiaphragmatic malformations, which include cardiac, renal, genital, and chromosomal abnormalities. Herein, we report a newborn born with concurrent congenital diaphragmatic hernia, Meckel's diverticulum, and heterotopic pancreatic tissue. This is the first case report of such a triad with description of possible mechanisms of the development.
    Language English
    Publishing date 2014-04-03
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2659094-3
    ISSN 2090-6811 ; 2090-6803
    ISSN (online) 2090-6811
    ISSN 2090-6803
    DOI 10.1155/2014/725945
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article: Congenital transmesenteric hernia in a neonate.

    Al-Shahwani, Noora / Al-Romaihi, Sheyma / J Ali, Mansour / Mandhan, Parkash

    Journal of neonatal surgery

    2015  Volume 4, Issue 1, Page(s) 9

    Language English
    Publishing date 2015-01-10
    Publishing country Pakistan
    Document type Journal Article
    ISSN 2226-0439
    ISSN 2226-0439
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Congenital mesenteric hernia in neonates: Still a dilemma.

    Mandhan, Parkash / Alshahwani, Noora / Al-Balushi, Zainab / Arain, Anwar

    African journal of paediatric surgery : AJPS

    2015  Volume 12, Issue 3, Page(s) 203–207

    Abstract: Congenital transmesenteric hernia in neonates is a rare cause of intestinal obstruction with devastating outcomes and still remains a challenge to diagnose pre-operatively. Patients are often managed with emergency surgical exploration and may need bowel ...

    Abstract Congenital transmesenteric hernia in neonates is a rare cause of intestinal obstruction with devastating outcomes and still remains a challenge to diagnose pre-operatively. Patients are often managed with emergency surgical exploration and may need bowel resection. We present 2 neonates with small bowel obstruction secondary to strangulated transmesenteric hernia through a congenital defect in the small bowel mesentery, which were managed successfully. We have also reviewed the literature about congenital transmesenteric hernia in neonates.
    MeSH term(s) Diagnosis, Differential ; Female ; Hernia/complications ; Hernia/congenital ; Hernia/diagnosis ; Herniorrhaphy ; Humans ; Infant, Newborn ; Intestinal Obstruction/diagnosis ; Intestinal Obstruction/etiology ; Intestinal Obstruction/surgery ; Intestine, Small ; Laparotomy ; Male ; Mesentery/abnormalities ; Radiography, Abdominal
    Language English
    Publishing date 2015-07
    Publishing country India
    Document type Case Reports ; Journal Article
    ZDB-ID 2392865-7
    ISSN 0974-5998 ; 0189-6725
    ISSN (online) 0974-5998
    ISSN 0189-6725
    DOI 10.4103/0189-6725.170231
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article: Infected hydrocele of the canal of nuck.

    Mandhan, Parkash / Raouf, Zaid / Bhatti, Khalid

    Case reports in urology

    2013  Volume 2013, Page(s) 275257

    Abstract: Hydrocele of the canal of Nuck in children is rare. It may present as incarcerated inguinal hernia and necessitates emergency exploration. Risk of infection in hydrocele of the canal of nuck is very rare. We present a case report of a 5-year-old girl who ...

    Abstract Hydrocele of the canal of Nuck in children is rare. It may present as incarcerated inguinal hernia and necessitates emergency exploration. Risk of infection in hydrocele of the canal of nuck is very rare. We present a case report of a 5-year-old girl who presented with a left tender inguinolabial region swelling with fever, tachycardia, and mild dehydration. The clinical features were suggestive of strangulated left inguinal hernia and further imaging and surgical exploration revealed it to be an infected hydrocele of the canal of Nuck. High ligation and hydrocelectomy were performed. Hydrocele of the canal of Nuck in a female child presenting with an inguinal swelling should be considered in differential diagnosis.
    Language English
    Publishing date 2013-12-04
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2627659-8
    ISSN 2090-6978 ; 2090-696X
    ISSN (online) 2090-6978
    ISSN 2090-696X
    DOI 10.1155/2013/275257
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Visceral basidiobolomycosis: An overlooked infection in immunocompetent children.

    Mandhan, Parkash / Hassan, Kamal Osman / Samaan, Sandra Moustafa / Ali, Mansour J

    African journal of paediatric surgery : AJPS

    2015  Volume 12, Issue 3, Page(s) 193–196

    Abstract: Visceral basidiobolomycosis is an unusual fungal infection of viscera caused by saprophyte Basidiobolus ranarum. It is very rare in healthy children and poses a diagnostic challenge due to the non-specific clinical presentation and the absence of ... ...

    Abstract Visceral basidiobolomycosis is an unusual fungal infection of viscera caused by saprophyte Basidiobolus ranarum. It is very rare in healthy children and poses a diagnostic challenge due to the non-specific clinical presentation and the absence of predisposing factors. We report a case of gastrointestinal basidiobolomycosis in a 4-year-old healthy girl who presented with a short history of abdominal pain, bleeding per rectum, fever, and weight loss. The diagnosis was based on high eosinophilic count, classical histopathology findings of fungal hyphae (the Splendore-Hoeppli phenomenon), and positive fungal culture from a tissue biopsy. Fungal infection was successfully eradicated with a combined approach of surgical resection of the infected tissue and a well-monitored course of antifungal therapy. The atypical clinical presentation, diagnostic techniques, and the role of surgery in the management of a rare and lethal fungal disease in an immunocompetent child are discussed.
    MeSH term(s) Child, Preschool ; Entomophthorales/isolation & purification ; Female ; Gastrointestinal Diseases/diagnosis ; Gastrointestinal Diseases/immunology ; Gastrointestinal Diseases/microbiology ; Humans ; Immunocompromised Host ; Zygomycosis/diagnosis ; Zygomycosis/immunology ; Zygomycosis/microbiology
    Language English
    Publishing date 2015-07
    Publishing country India
    Document type Case Reports ; Journal Article
    ZDB-ID 2392865-7
    ISSN 0974-5998 ; 0189-6725
    ISSN (online) 0974-5998
    ISSN 0189-6725
    DOI 10.4103/0189-6725.170218
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article: Complicated Amyand's Hernia in a Neonate.

    Mandhan, Parkash / Al Rayes, Talal / J Ali, Mansour / Aldhaheri, Mahmoud

    Journal of neonatal surgery

    2014  Volume 3, Issue 3, Page(s) 38

    Abstract: Amyand's hernia is a rare clinical entity in which the vermiform appendix is present within the inguinal hernia sac. Here, we report a 5-day-old neonate with dysmorphic features referred to us with a tender irreducible right inguino-scrotal swelling. ... ...

    Abstract Amyand's hernia is a rare clinical entity in which the vermiform appendix is present within the inguinal hernia sac. Here, we report a 5-day-old neonate with dysmorphic features referred to us with a tender irreducible right inguino-scrotal swelling. Surgical exploration showed gangrenous appendix with a peri-appendicular abscess in the inguinal hernia sac. Appendectomy and right herniotomy was performed.
    Language English
    Publishing date 2014-07-10
    Publishing country Pakistan
    Document type Case Reports
    ISSN 2226-0439
    ISSN 2226-0439
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: Infected Hydrocele of the Canal of Nuck

    Parkash Mandhan / Zaid Raouf / Khalid Bhatti

    Case Reports in Urology, Vol

    2013  Volume 2013

    Keywords Diseases of the genitourinary system. Urology ; RC870-923 ; Specialties of internal medicine ; RC581-951 ; Internal medicine ; RC31-1245 ; Medicine ; R ; DOAJ:Urology ; DOAJ:Medicine (General) ; DOAJ:Health Sciences
    Language English
    Publishing date 2013-01-01T00:00:00Z
    Publisher Hindawi Publishing Corporation
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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