8 results match your criteria: "The Children's Hospital and ICH[Affiliation]"
J Coll Physicians Surg Pak
September 2021
Department of Paediatric Medicine, The Children's Hospital and ICH, Lahore, Pakistan.
Objective: To explore the reflective capacity as a learning tool in pediatric residents.
Study Design: Survey.
Place And Duration Of Study: The Children's Hospital Lahore, Pakistan from 20th March to 30th March 2021.
J Coll Physicians Surg Pak
September 2017
Department of Pediatric Hematology/Oncology, The Children's Hospital and ICH, Lahore.
Hodgkin Lymphoma (HL) is a lymphoid tumour that represents about 1% of all neoplasms occurring worldwide. HLis the most treatable of childhood malignancies. The etiology of HLis unknown.
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May 2017
Department of Pediatrics, Lahore General Hospital/PGMI, Lahore.
Paraneoplastic syndromes are rare disorders that are triggered by an altered immune system response to neoplasm. Paraneoplastic syndromes may be the first or the most prominent manifestations of cancer. Wilm's tumor is the most frequent pediatric renal malignancy and usually presents with abdominal mass.
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September 2016
Department of Paediatric Endocrinology, The Children's Hospital and ICH, Lahore.
Allgrove syndrome or triple-Asyndrome is a rare familial multisystem autosomal recessive disorder. It is characterised by triad of alacrima, achalasia and adrenal insufficiency due to adrenocorticotropin hormone (ACTH) resistance. If it is associated with autonomic dysfunction, it is termed as 4-Asyndrome.
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October 2015
Department of Paediatrics. Lahore General Hospital/PGMI, Lahore.
Ollier's disease also known as enchondromatosis is a rare skeletal disorder that is usually sporadic, non-hereditary, and characterized by abnormal bone development (skeletal dysplasia). While this disorder may be present at birth (congenital); it may not become apparent until early childhood with more obvious symptoms, such as deformities or improper limb growth. It carries high risk of skeletal, visceral and brain malignancy seen in approximately 25% of patients.
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July 2015
Department of Paediatric Medicine, The Children's Hospital and ICH, Lahore.
Pulmonary Alveolar Proteinosis (PAP) is a rare syndrome in the paediatric age group and characterized by intra-alveolar accumulation of proteinaceous phospholipid-laden material called surfactant. The diagnosis is made by High Resolution Computed Tomography (HRCT) chest which shows characteristic crazy paving appearance and diagnosis confirmed by Bronchoalveolar Lavage (BAL). We report two cases.
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March 2014
Department of Paediatrics, Lahore General Hospital / PGMI, Lahore.
Ewing's sarcoma, a primitive neuroectodermal tumour is a rare entity belonging to a family of neoplasms of neuroectodermal origin. These highly aggressive neoplasms primarily affect older children and young adults. They primarily involve the bones or soft tissues.
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August 2012
Department of Paediatric Critical Care Unit, The Children's Hospital and ICH, Lahore.
Pheochromocytomas are rare neuroendocrine tumours of chromaffin tissues. They are catecholamine secreting tumours which cause severe hypertension and other systemic disturbances. Of all the causes of childhood hypertension, pheochromocytoma constitutes less than 1%.
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