517 results match your criteria: "Army Hospital - Research and Referral[Affiliation]"

We describe a novel technique for recurrent pterygium and assess the advantage of properties of extended tenonectomy, amniotic membrane transplantation, and limbal epithelial transplantation in terms of recurrence rate, postoperative symptoms, postoperative orthoptics, and other complications. A total of nine eyes with recurrent pterygium underwent PERMISLET, i.e.

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Background: 'Breast cancer' the most common cancer amongst females in India. Having good Quality of life (QoL) among the patients undergoing treatment is one of the vital and significant factors for ensuring holistic approach to treatment and well-being of cancer patients. The present study was conducted to assess the QoL and its determinants among breast cancer patients undergoing treatment at a tertiary care institute in western Maharashtra.

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Interstitial pregnancy accounts for only 2%-4% of all ectopic pregnancies, however, it is associated with higher mortality rates as compared to other ectopic pregnancies, due to the associated risk of uterine rupture, and hemorrhage. A 35-year-old gravida 4 abortion 3 woman reported at the 8 week of gestation for antenatal care with comorbidity of protein C and protein S deficiency and recurrent pregnancy loss with for routine care. She was diagnosed as a case of interstitial pregnancy by transvaginal sonography and magnetic resonance imaging.

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Pulmonary thromboembolism (PTE) is a life-threatening illness. It is a great masquerader that mimics many respiratory illnesses, warranting a high index of suspicion for diagnosis. It should be suspected when respiratory illnesses do not respond to the expected course of treatment.

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HLA-B*13:01:01:12 differs from HLA-B*13:01:01:01 by a single nucleotide.

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Article Synopsis
  • - Phenotypic plasticity in tumor cells allows them to adapt and change due to stressors, playing a key role in tumor progression, as illustrated by a case of a 70-year-old man with pleomorphic adenoma who developed pleomorphic liposarcoma.
  • - Sarcomas, like liposarcoma, can develop from existing pleomorphic adenomas in the parotid gland, with only a few documented cases of primary parotid liposarcoma.
  • - This case report examines the uncharted adenoma-carcinoma-sarcoma progression in pleomorphic adenomas, aiming to provide insights for treatment planning and management from a surgical oncology standpoint.
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As genetic testing becomes increasingly accessible and affordable, the uniform and accurate interpretation of genetic variants becomes essential. The ACMG/AMP joint guidelines provide the basis for systematic and uniform interpretation of pathogenicity of genetic variants. However, the application of these in routine clinical interpretation at-scale has largely been limited by the lack of resources providing harmonized data especially at a population-scale.

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Mycosis fungoides (MF) is the most common type of cutaneous T-cell lymphoma in adults. However, it is rare in middle childhood. Such cases usually present with hypopigmented patches that may mimic common childhood dermatoses, thereby causing a delay in the diagnosis.

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Purpose: This study aims to renew the management of viral epidemic conjunctivitis by introducing a one-time, low-concentration ocular surface povidone-iodine (LOS-pI) wash.

Methods: Among the 3,002 patients screened, 1,328 with acute conjunctivitis were categorized into two groups. Group A (664 patients) underwent a 1% betadine wash in addition to the standard treatment protocol (Eye Lubricant + Moxifloxacin 0.

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KBG Syndrome in 16 Indian Individuals.

Am J Med Genet A

October 2024

Suma Genomics Private Limited, Manipal, India.

Article Synopsis
  • - The study analyzed the clinical and genetic features of 16 individuals with KBG syndrome (KBGS) from 13 Indian families, focusing on likely pathogenic variants in the ANKRD11 gene.
  • - Key clinical traits observed included a high prevalence of learning/intellectual disabilities (93%), skeletal abnormalities (93%), and distinctive facial features (87%).
  • - Genetic analysis revealed 12 single nucleotide variants (SNVs) in the ANKRD11 gene, with many clustering around exon 9, and the Face2Gene application showed high accuracy in suggesting differential diagnoses for KBGS.
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  • This prospective observational study assessed the depth of the mastoid antrum using High Resolution Computed Tomography (HRCT) and during surgery in 35 patients undergoing mastoidectomy at a military hospital.
  • The average depth measured was similar between HRCT (1.625 cm) and surgical measurements (1.651 cm), with significant findings about differences in depth based on age and the presence of Koerner's Septum, but not on gender or specific disease types.
  • Ultimately, 82.3% of pediatric and 82.9% of adult patients had deeper mastoid antrum measurements than the standard depth, indicating anatomical variations that may need consideration in clinical practice.
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Screening for Fabry disease in patients on Hemodialysis.

Int J Appl Basic Med Res

August 2024

Division of Clinical Genetics, Department of Paediatrics, Army Hospital Research and Referral, New Delhi, India.

Background: Fabry disease is an under-recognized X-linked lysosomal storage disorder characterized by the accumulation of trihexosylceramides in multifarious tissues, leading to end-organ damage, including progressive renal failure. Antecedent screening studies worldwide have shown inconsistent prevalence in the hemodialysis population. We conducted this study to screen for Fabry disease in patients undergoing dialysis at a tertiary care hospital.

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Article Synopsis
  • Wolfram syndrome (WS) is a rare genetic disorder featuring a combination of symptoms like diabetes, optic atrophy, and hearing loss, primarily caused by a deficiency in arginine vasopressin.
  • The case describes an early adolescent girl initially diagnosed with type 1 diabetes, who later presented with urinary issues and vision problems, leading to the discovery of optic atrophy and chronic kidney disease.
  • Although she didn't exhibit all typical symptoms of WS, such as deafness, her case highlighted the need for thorough evaluation in juvenile diabetes patients, as early renal involvement could indicate conditions beyond common complications.
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Article Synopsis
  • Advances in immuno-oncology have improved treatment for renal cell carcinoma, but patients with "primary refractory" disease have poor outcomes; our study found a 19% prevalence of this group among 1,709 metastatic clear cell patients across 72 centers in 22 countries.
  • The highest primary refractory rate was 27% with nivolumab/ipilimumab, while pembrolizumab/lenvatinib had the lowest at 10%; those classified as primary refractory only had a median survival of 7.6 months compared to 55.7 months for non-primary refractory patients.
  • Significant predictors of survival for primary refractory patients included factors like prior nephrectomy and presence of bone/brain metastases, highlighting the complex
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Background: The objectives of this study were to bring out the results of application of pleural wrap in primary repair of tracheo - esophageal fistula (TEF) with long-gap oesophageal atresia (LGEA) and also define the role of neonatologists and paediatric intensivists in post-operative management in these patients by laying down standard neonatal management protocol.

Materials And Methods: This was a retrospective descriptive observational study conducted between March 2011 and April 2019 on 23 cases of LGEA with TEF. The study was conducted at two tertiary care paediatric surgery centres in Northern part of India wherein these newborn babies were operated by two paediatric surgeons with variable experience of 8-12 years.

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During the COVID-19 pandemic, our findings highlight changes in AML management strategies in India. There was a decrease in overall patient registrations, particularly at large referral centers, while smaller centers saw an increase, reflecting a shift towards more localized care. This shift was accompanied by a rise in the use of hypomethylating agents (HMAs).

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Article Synopsis
  • - Angioid streaks are irregular breaks in Bruch's membrane, appearing as pigmented lines that can indicate underlying systemic diseases like pseudoxanthoma elasticum, Paget's disease, and hemoglobinopathies in about 50% of cases, though some may be idiopathic.
  • - Patients often remain asymptomatic until complications arise, such as choroidal neovascular membrane or subretinal hemorrhage, which can occur even from minor trauma due to the membrane's fragility.
  • - Diagnosis involves clinical exams and imaging techniques like fundus autofluorescence and optical coherence tomography, while treatment typically focuses on managing complications, often through intravitreal injections of antivascular endothelial growth factor.
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Hepatocellular carcinoma (HCC) is an extremely rare long-term complication of Budd-Chiari syndrome (BCS) which may occur due to long-term venous congestion causing fibrosis, cirrhosis and subsequent hepatocellular dysplasia or anaplasia. This complication is even rarer in paediatric BCS and warrants early diagnosis for a favourable prognosis. Benign regenerative nodules seen with BCS are difficult to differentiate from malignant nodular lesion of HCC, thereby making serial imaging less sensitive for early diagnosis of HCC in BCS.

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Background In today's era of anesthesia, balanced anesthesia is the main basis of patient care and pain management. Of all the medications given during general anesthesia, premedication, induction agents, and muscle relaxants play a major role in keeping the hemodynamics properly under control. When laryngoscopy is performed to intubate, a pain stimulus will be generated, leading to a rise in blood pressure and heart rate.

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HLA-C*17:78 differs from HLA-C*17:03:01:03 by one nucleotide change C>T in exon 3 (GCG>GTG).

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