SUBMIT YOUR MANUSCRIPT

VOLUME 3, YEAR 2025

Aims & Scope

JCPSP Case Reports is a peer-reviewed online-only journal by the College of Physicians and Surgeons Pakistan (CPSP). The journal publishes original case reports in all fields of Medical Sciences. The purpose of JCPSP Case Reports is to provide clinicians and researchers, in particular postgraduate trainees and fellows of CPSP, a forum to publish their unique experiences to a wide readership for the advancement of clinical acumen.

Latest Articles
Volume 3 | Year 2025
Looking Ahead – A New Year of Growth and Innovation for JCPSP Case Reports

By Muhammad Shoaib Shafi

Page #: 1-1


Familial Achalasia Cardia in Childhood: A Case Report of Three Siblings

By Hamza Malik, Sajid Iqbal Nayyar, Wajeeh Ur Rehman, Faryal Iqbal, Nabila Talat

Page #: 126-127

ABSTRACT Achalasia cardia is a rare condition in the paediatric population, and familial occurrences are even rarer. The authors herein report a case of three siblings diagnosed with familial achalasia cardia. The first case was a 12-year male who presented with progressive dysphagia to solids and l...


Pancreatic Tuberculosis: An Unusual Site for a Common Illness

By Shahid Sarwar, Muhammad Moeed Akram, Sabeen Farhan, Ghulam Abbas, Yasir Mahmud

Page #: 128-130

ABSTRACT Tuberculosis (TB) of the pancreas is a rare form of extra-pulmonary tuberculosis that needs a high index of clinical suspicion and in most cases is wrongly diagnosed as pancreatic carcinoma due to the presence of space-occupying lesions in the majority of these patients. Hence, diagnosis of...


Minimal Change Disease Induced by Rifampicin: A Case Report

By Ke-Ping Han, Li-Hua Li, Lin Yang

Page #: 131-133

ABSTRACT Rifampicin, the medicine used for the treatment of tuberculosis (TB), has the potential to causekidney damage, most commonly manifested as acute interstitial nephritis. The potential of causing minimal change disease (MCD) of the kidney is very rare, and it is often relieved after the use o...


A Rare Case Report of Rapunzel Syndrome with Multiple Small Gut Intusseceptions

By Ahmed Siddique Ammar, Faryal Ufaq, Mehvish Irshad, Muhammad Shoaib, Muhammad Saud Iqbal

Page #: 134-136

ABSTRACT Rapunzel syndrome (RS) is a condition defined as the presence of trichobezoar in the form of hair. It is found in patients with psychiatric disorders called trichotillomania (the habit of pulling hair) and trichophagia (repeated ingestion of hair). Children with pica eat non- digestible thi...


Unveiling the Unseen: A Rare Case of Brain Metastatic Ewing Sarcoma Originating in the Spinal Cord

By Cheng Xie, Ye Song, Qianliang Huang

Page #: 137-139

ABSTRACT Ewing sarcoma (ES) with brain metastasis is an uncommon clinical occurrence, generally arising from primary tumours located in the skull or the long bones of the extremities. This report documents an extraordinarily rare instance of brain metastatic ES (BMES), with the primary neoplasm situ...


Successful Recovery of a Patient with Congenital Heart Disease and ARDS after Drowning with Veno-Venous ECMO Support

By Ruqin Yi, Zhaokun Fan

Page #: 140-143

ABSTRACT This paper presents a rare case of acute respiratory distress syndrome (ARDS) induced by drowning in a 24-year male student with a history of congenital heart disease (CHD), who showed substantial neurological recovery after receiving cardiopulmonary resuscitation (CPR) and veno-venous extr...


Unilateral Primary Orbital Malignancy in a Seven-Month Child

By Murtaza Sameen, Zahra Arsalan, Huda Mir, Fariha Taimur, Tayyab Afghani

Page #: 144-146

ABSTRACT Progressive unilateral primary proptosis is extremely rare in a newborn. There are different points to differentiate between inflammatory disease process, infectious cause, vascular lesion, endocrine lesion, and neoplastic lesion. The presented case will further elaborate on the features of...


Furuncular Myiasis: A Diagnostic Challenge in Non-Endemic Regions

By Atiya Rahman, Samra Iram, Nazia Rashid

Page #: 147-149

ABSTRACT Myiasis is a rare infestation caused by the larvae (maggots) of fly species. Due to frequent travelling, diseases previously restricted to certain parts of the world are being encountered in non-endemic areas. We report a case of a young Pakistani who had a history of travelling to Africa. ...


Bronchoscopic Resection of Inflammatory Myofibroblastic Tumour: A Rare Cause of Recurrent Haemoptysis and Lobar Atelectasis

By Talha Mahmud, Syed Naveed Tahir

Page #: 150-152

ABSTRACT This case report presents a rare example of a benign inflammatory myofibroblastic tumour (IMT) in the bronchus, highlighting the importance of a thorough diagnostic work-up and successful bronchoscopic resection without surgery. A 25-year female patient presented with low-grade fever, progr...


Laparoscopic-Assisted Trans-Anal Removal of Self-Inserted Foreign Body in the Sigmoid Colon: A Case Report and Literature Review

By Zhen Liu, Lu Ren, Enrui Liu, Xingang Peng

Page #: 153-155

ABSTRACT We report a rare case of a 16-year male teenager who initially presented with abdominal bloating as the result of a self-inserted cylindrical- shaped metal tin in his sigmoid colon. The patient denied any history of psychiatric disease. He also denied any drug abuse or previous comorbiditie...


Unravelling the Coexistence of Incomplete Pancreatic Divisum and Choledochal Cyst

By Mariam Shah, Aroosa Kanwal, Laiba Masood, Sajida Shah

Page #: 156-158

ABSTRACT Choledochal cysts are rare congenital cystic dilatations of the biliary tree. Pancreatic divisum is the most common anomaly of the pancreatic ductal system, characterised by the dorsal pancreatic duct functioning as the primary drainage channel, with the majority of secretions draining thro...


Lichenoid Pseudovesicular Papular Eruption on Nose (LIPEN): A Case Report

By Ayesha Zahir, Sadaf Ahmed Asim, Madiha Sajid

Page #: 159-161

ABSTRACT Papules located over the face have a wide range of differential diagnoses. Differentiation on clinical grounds is often difficult requiring histopathological correlation. Despite diagnostic and therapeutic advancements in dermatology, certain conditions continue to pose diagnostic challenge...


Two Cases of IgA Nephropathy in Patients Receiving Infliximab for Crohn's Disease

By Zhuohan Xu, Lingzhi He

Page #: 162-164

Abstract IgA nephropathy (IgAN) represents the most widespread type of primary glomerulonephritis across the globe, notable for the deposition of IgA within the glomerular mesangial region. Infliximab, a monoclonal antibody developed to precisely target tumour necrosis factor alpha (TNF-α), ha...


Lucio’s Leprosy: A Different Presentation of Hansen’s Disease

By Madiha Sajid, Ayesha Zahir, Sadaf Ahmed Asim, Eraj Aman, Sharmin Nasir

Page #: 165-167

ABSTRACT Lucio’s leprosy is a distinct form of lepromatous leprosy characterised by non-nodular diffuse cutaneous involvement. Despite being endemic in underdeveloped countries, this particular form of leprosy is rarely reported outside the Mexico and Costa Rica. Owing to the absence of speci...


Presacral Epidermoid Cyst in a Child with Anorectal Malformation: An Incomplete Currarino Triad

By Sana Viqar, Sadia Asmat Burki, Muhammad Amjad Chaudhary

Page #: 168-170

ABSTRACT Currarino syndrome is a hereditary disorder characterised by a triad of anorectal malformation (ARM), sacral vertebral defect, and pre-sacral mass. An incomplete triad may also be present due to a variable phenotype. Presacral masses in children often include a number of differential diagno...


Resolution of Optic Disc Pit Maculopathy with Topical Brinzolamide and Nepafenac: A Case Report and Literature Review

By Arshad Mehmood, Muhammad Abdul Rehman Siddiqui

Page #: 171-173

ABSTRACT Optic disc pit (ODP) is a rare ocular congenital anomaly. Fluid from the optic disc enters retinal layers, causing retinoschisis and inverse lamellar holes. This results in gradual visual loss. Various treatments have been tried in ODP-maculopathy (ODP-M). An early adolescent female present...


Anaesthesia Management of a Patient with Severe Regurgitative Lesion and Right Heart Failure Posted for Open Cholecystectomy under Erector Spinae and Transverse Abdominis Plane Blocks

By Aleena Kashif, Kashif Mumtaz Bhatti, Jodat Saleem, Sami Ur Rehman, Zeeshan Kashif

Page #: 174-177

ABSTRACT Mitral regurgitation affects 2% of the world’s population. Patients with pulmonary hypertension (PH) and right heart failure indicate a poor prognosis, which necessitates the need for early surgical intervention. The authors present a case of a patient with severe mitral regurgitation...


Anaesthesia Management of a Patient with Congenital Kyphoscoliosis and Large Atrial Septal Defect Posted for Kyphoscoliosis Corrective Surgery

By Sami Ur Rehman, Ahmed Masood, Asim Razaaq, Khawar Ali

Page #: 178-180

ABSTRACT The authors present the anaesthesia management of a 12-year female patient who underwent corrective surgery for kyphoscoliosis under general anaesthesia. The patient had congenital idiopathic kyphoscoliosis with left lateral curvature (left convex), C7-hemivertebrae, large atrial septal def...


Facial Lupus Vulgaris Exhibiting Recurrent Purulent Discharge: An Unusual Presentation

By Atiya Rahman, Madeeha Asrar, Lalain Masood

Page #: 181-184

ABSTRACT Cutaneous disorders can run a chronic course and can be quite disfiguring on the exposed body parts, such as the face and hands. Due to the low prevalence of cutaneous tuberculosis, physicians might be unfamiliar with unusual presentations, leading to such infections going undiagnosed for y...


Correlation Between Toripalimab Immune Therapy and Vitiligo: A Case Report of Complete Response and Adverse Reactions in Advanced Stage Melanoma of Unknown Primary

By Tiantian Zhang, Yufo Chen, Yumei Li, Yang Liu, Rui Wang

Page #: 185-188

ABSTRACT Melanoma of unknown primary (MUP) is a rare subtype of melanoma, accounting for approximately 3% of cases and characterised by metastasis in the absence of a detectable primary lesion. This report describes the case of a stage IV MUP patient with a BRAF V600E mutation who developed vitiligo...


« ‹ Previous Page 3 of 5 Pages Next › »