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Your search keyword '"Lakshpaul Chauhan"' showing total 4 results
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4 results on '"Lakshpaul Chauhan"'

1. Complete Eye Ophthalmoplegia: the unusual initial presentation of Leptomeningeal Carcinomatosis

Author

Lakshpaul Chauhan, Ateeq Mubarik, Abdulmagid Eddib, Mohammad Eid, Ali Vaziri, and Salman Muddassir

Subjects
Ophthalmoplegia, Leptomeningeal Carcinomatosis, large B-cell lymphoma, non-hodgkin lymphoma, Internal medicine, RC31-1245
Abstract

Ophthalmoplegia is a paralysis or weakness of extraocular muscles that have a variety of different etiologies including and not limited to Leptomeningeal Carcinomatosis (LC). LC is caused mainly by metastatic cancers and can cause a wide variety of symptoms. We present a case of LC with no preexisting condition who presented with a unilateral ophthalmoplegia as initial presentation who was found to have LC secondary to large B-cell lymphoma.

Published
2019
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2. Pulmonary arterial hypertension: A rare yet fatal complication of Neurofibromatosis Type 1

Author

Melanie Rojas, Ateeq Mubarik, Elizabeth Ann Henderson, Fatima Agha, Lakshpaul Chauhan, Arshad Muhammad Iqbal, Ali Vaziri, and Salman Muddassir

Subjects
Diseases of the respiratory system, RC705-779
Abstract

Neurofibromatosis Type 1 (NF1) is an autosomal dominant genetic disorder with an incidence of approximately 1 in 4,000 live births [1]. Pulmonary arterial hypertension (PAH) is a rare but extremely life-threatening complication associated with NF1. Timely recognition of this unusual and severe association between NF1 and PAH is imperative in prolonging the survival in this specific patient population. We present the clinical outcomes of a 47-year old female previously diagnosed with NF1, who presented with progressively worsening dyspnea. Keywords: NF1, PAH, PH

Published
2019
Full Text
View/download PDF

3. Complete Eye Ophthalmoplegia: the unusual initial presentation of Leptomeningeal Carcinomatosis

Author

Abdulmagid Eddib, Ali Vaziri, Ateeq Mubarik, Lakshpaul Chauhan, Salman Muddassir, and Mohammad Eid

Subjects
Pathology, medicine.medical_specialty, Weakness, lcsh:Internal medicine, genetic structures, Case Report, non-hodgkin lymphoma, 030204 cardiovascular system & hematology, Extraocular muscles, 03 medical and health sciences, 0302 clinical medicine, Internal Medicine, Paralysis, Medicine, 030212 general & internal medicine, lcsh:RC31-1245, Ophthalmoplegia, large B-cell lymphoma, business.industry, eye diseases, Leptomeningeal Carcinomatosis, medicine.anatomical_structure, sense organs, Presentation (obstetrics), medicine.symptom, business
Abstract

Ophthalmoplegia is a paralysis or weakness of extraocular muscles that have a variety of different etiologies including and not limited to Leptomeningeal Carcinomatosis (LC). LC is caused mainly by metastatic cancers and can cause a wide variety of symptoms. We present a case of LC with no preexisting condition who presented with a unilateral ophthalmoplegia as initial presentation who was found to have LC secondary to large B-cell lymphoma.

Published
2019

4. Pulmonary arterial hypertension: A rare yet fatal complication of Neurofibromatosis Type 1

Author

Arshad Iqbal, Salman Muddassir, Ateeq Mubarik, Melanie Rojas, Ali Vaziri, Elizabeth Henderson Md, Fatima Agha, and Lakshpaul Chauhan

Subjects
Pulmonary and Respiratory Medicine, Pediatrics, medicine.medical_specialty, congenital, hereditary, and neonatal diseases and abnormalities, PH, Article, 03 medical and health sciences, 0302 clinical medicine, Medicine, Neurofibromatosis, neoplasms, lcsh:RC705-779, business.industry, Incidence (epidemiology), Genetic disorder, lcsh:Diseases of the respiratory system, PAH, medicine.disease, eye diseases, nervous system diseases, Patient population, 030228 respiratory system, NF1, 030220 oncology & carcinogenesis, business, Complication
Abstract

Neurofibromatosis Type 1 (NF1) is an autosomal dominant genetic disorder with an incidence of approximately 1 in 4,000 live births [1]. Pulmonary arterial hypertension (PAH) is a rare but extremely life-threatening complication associated with NF1. Timely recognition of this unusual and severe association between NF1 and PAH is imperative in prolonging the survival in this specific patient population. We present the clinical outcomes of a 47-year old female previously diagnosed with NF1, who presented with progressively worsening dyspnea. Keywords: NF1, PAH, PH

Published
2019

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