Case Reports · Vol. 6 No. 2 (2015)

Spinal Primitive Neuroectodermal Tumor in Children A rare case report and literature review

Cover
JPSB
Journal of
Paediatric Surgeons of Bangladesh
Published : July 2015
CONTENTSVolume 06Number 2July 2015
Editorial
Counselling of Parents, attendants, guardians in dealing of Paediatric Surgical Patients
Kazi Habibur Rahman
32
Review Articles
Hemophilia in Children
Shahnoor Islam, AKM Amirul Morshed, Zohora Jameela Khan
54
Original Articles
Three Years Experience of Inguinal Hernia in Children in BSMMU
Shoheli Alam, KM Didarul Islam, Abu Saleh Md Oli Ullah, Md Tosaddeque Hossain Siddiqui, Md Ruhul Amin
34
Outcome of Partial Splenectomy for Hypersplenism in Children with Thalassemia
Mizanur Rahman, Susankar Kumar Mondal, Amin Lutful Kabir, Md Ruhul Amin, Matiur Rahman
39
Abdominal Ultrasonography and Radiography Diagnosis in Preterm Necrotizing Enterocolitis
S Tuya, Ch Battulga, TS Tsogtsolmaa, M Tumennasan, N Davaatseren, Kaniz Hasina
47
Case Reports
Spinal Primitive Neuroectodermal Tumor in Children A rare case report and literature review
AKM Amirul Morshed, Shahnoor Islam, Sayeeda Anwar
64
The Official Journal of the
ASSOCIATION OF PAEDIATRIC SURGEONS OF BANGLADESH (APSB)
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Authors

  • AKM Amirul MorshedAssociate Professor and Head, dept of Pediatric Hematology and oncology, Dhaka medical College, Dhaka
  • Shahnoor IslamAssociate Professor, dept of Pediatric Surgery, Dhaka medical College, Dhaka
  • Sayeeda AnwarProfessor and Head, Dept of Pediatric Nephrology, Dhaka medical College, Dhaka

Keywords

Abstract

Primitive neuroectodectodermal tumor is a rare tumor in childhood. It is aggressive childhood malignancies and offer a significant challenge to treatment. An eleven year old female baby presented with fever, pain and neurologic manifestation. Initialy it was diagnose as TB vertebrae and treated accordingly but no improvment rather new metastatic swelling appear after few days. Diagnosis was made by MRI and local tissue biopsy and immunohistohistochemistry. As it is rare and highly invasssive malignancy with poor out come the case was presented along with literature review.

Journal of Paediatric Surgeons of Bangladesh (2015) Vol. 6 (2): 64–67

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