APSP Journal of Case Reports 2018-09-22T08:15:43-04:00 Prof. Jamshed Akhtar Open Journal Systems <p>APSP Journal of Case Reports is owned and published by The Association of Paediatric Surgeons of Pakistan (Registered). APSP J Case Rep is an open access, peer reviewed electronic journal. Our primary mission is to provide a portal for residents in training and junior consultants to get their research published. The journal also provides an open access forum for research scholars to publish high quality case reports that in turn would serve to disseminate manuscripts of clinical value without any barriers of subscription. Case Reports from all across the globe are accepted and published after rigorous peer review. This shall be a learning opportunity as well. It will also help in developing research culture.&nbsp;<br>All articles appearing in this publication, including editorials, letters etc represent the opinions of the authors and do not necessarily reflect the official policy or opinions of the APSP. Acceptance of any and all articles and advertisement in this publication or any other material published by APSP Journal of Case Reports does not imply endorsement by the publisher or APSP.&nbsp;APSP J Case Rep disclaims any liability to any party for the accuracy, completeness, or availability of any and all publications and other material, or for any damages arising out of the use or nonuse of this publication, and any and all publications (and other material), and any information&nbsp; (and other material), and any information contained therein.</p> Single System Ectopic Congenital Giant Megaureter Associated with Ipsilateral Multicystic Dysplastic Kidney 2018-09-22T08:15:42-04:00 Santosh Kumar Mahalik Bikasha Bihary Tripathy Akash Bihari Pati Manoj Kumar Mohanty <p>Congenital anomalies of the kidney and urinary tract (CAKUT) is a disease spectrum of a wide range of structural and functional anomalies. In this report, we have presented a rare case of CAKUT displaying the wide spectrum of renal and urinary tract anomalies with an unusual association like single system ectopic giant <em>megaureter</em> with the ipsilateral multicystic dysplastic kidney.</p> 2018-06-19T12:48:39-04:00 ##submission.copyrightStatement## Congenital Anterior Urethrocutaneous Fistula: Report of Three Cases 2018-09-22T08:15:42-04:00 Akash Bihari Pati Santosh Kumar Mahallik Bikasha Bihary Tripathy Manoj Kumar Mohanty <p>The Congenital anterior urethrocutaneous fistula is a rare entity with varied anatomic configurations. In this report, we present three different varieties of congenital anterior urethrocutaneous fistula. The anterior urethrocutaneous fistula was associated with no urethra, hypoplastic urethra, and normal urethra, distal to fistula, 1 in each patient. Each required a different treatment strategy. Postoperative outcome was good in all cases.</p> 2018-06-18T21:56:35-04:00 ##submission.copyrightStatement## Multiple Congenital Granular Cell Tumor in a Neonate - A Rare Case 2018-09-22T08:15:42-04:00 Aditya Pratap Singh Arun Kumar Gupta Maryem Ansari Ramesh Tanger Dinesh Kumar Barolia <p>Congenital granular cell tumor (CGCT) is an uncommon congenital benign epulis in neonates. A preliminary diagnosis is usually put forth clinically but may be confused with other anomalies. Herein, we report an unusual case of intra oral congenital granular cell tumor in a 4-day-old female newborn. The tumor was excised completely. At 3-month follow-up, the baby is doing fine without any recurrence.</p> 2018-06-18T21:26:36-04:00 ##submission.copyrightStatement## Penile Cutaneous Horn 2018-09-22T08:15:42-04:00 Namita Bhutani Pradeep Kajal 2018-06-18T20:53:23-04:00 ##submission.copyrightStatement## Desmoid Tumor of the Rectus Abdominis Muscle in a 2-Year-Old Boy 2018-09-22T08:15:43-04:00 Asmir Jonuzi Zlatan Zvizdic Nusret Popovic Emir Milisic Azra Karamustafic Amira Mesic Irmina Sefić Amra Džananović <p>Aggressive fibromatosis, also known as desmoid tumor, is a locally invasive soft tissue lesion arising from connective tissues. Reports in children less than 10 years of age is rare. We report a case of a&nbsp; desmoid tumor located at the middle and lower third of the left rectus abdominis, in a 2-year-old-boy. Partial resection of the muscle segment and simultaneous reconstruction of the abdominal wall by abdominal fascia was done. The patient had an uneventful recovery. At one year of follow-up neither recurrence nor functional or aesthetic complications were seen.</p> 2018-06-18T20:52:20-04:00 ##submission.copyrightStatement##