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10 results on '"Halder, Chinmay"'

1. A clinical rating scale for the assessment of facial aging in Indian population

Author

Sen, Sumit, Choudhury, Supriyo, Gangopadhyay, Anusree, Halder, Chinmay, Biswas, Projna, and Jain, Atul

Subjects
Aging -- Research, Skin -- Care and treatment, Health
Abstract

Byline: Sumit. Sen, Supriyo. Choudhury, Anusree. Gangopadhyay, Chinmay. Halder, Projna. Biswas, Atul. Jain Background: Estimation of facial aging has assumed growing importance due to the advent of several antiaging therapies. [...]

Published
2016

2. Hemilateral proteus syndrome: An unusual hamartomatous disorder with significant cerebellar tonsillar herniation

Author

Saha, Archana, Halder, Chinmay, Sen, Sumit, and Chatterjee, Gobinda

Subjects
Proteus syndrome -- Diagnosis -- Care and treatment -- Case studies, Health
Abstract

Byline: Archana. Saha, Chinmay. Halder, Sumit. Sen, Gobinda. Chatterjee Sir, A 14-year-old boy, born to nonconsanguineous parents following normal pregnancy, presented to the outpatient clinic with asymmetry of limbs, linear [...]

Published
2015

3. Granuloma faciale: Exclusively extrafacial

Author

Trupti V Surana, Ghosh Arghyaprasun, Biswas Saugato, Nag Falguni, Chatterjee Gobinda, and Halder Chinmay

Subjects
Extrafacial, granuloma faciale, grenz zone, polymorphous infiltrate, Dermatology, RL1-803
Abstract

We report a case of granuloma faciale over distal extremities in a 60-year-old man without facial lesions who did not show any response to dapsone.

Published
2013
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4. Phakomatosis pigmentovascularis presenting with Sturge-Weber syndrome and Klippel-Trenaunay syndrome

Author

Sen, Sumit, Bala, Sanchaita, Halder, Chinmay, Ahar, Rahul, and Gangopadhyay, Anusree

Subjects
Angiomatosis -- Case studies, Sturge-Weber syndrome -- Case studies, Rare diseases -- Case studies, Health
Abstract

Byline: Sumit. Sen, Sanchaita. Bala, Chinmay. Halder, Rahul. Ahar, Anusree. Gangopadhyay Phakomatosis pigmentovascularis (PPV) is a rare cutaneous disorder characterized by combination of capillary malformation and other pigmented naevi. Four [...]

Published
2015

5. Eccrine angiomatous hamartoma: late onset facial presentation

Author

Halder, Chinmay, Naskar, Biswanath, Biswas, Projna, and Mitra, Pradip

Subjects
Sweat glands -- Diseases, Hamartoma -- Diagnosis -- Case studies -- Reports, Health
Abstract

Byline: Chinmay. Halder, Biswanath. Naskar, Projna. Biswas, Pradip. Mitra Eccrine angiomatous hamartoma (EAH) is a very rare benign neoplastic condition characterized by hamartomatous proliferation of eccrine glands and accompanying blood [...]

Published
2014

6. Zosteriform palisaded encapsulated neuroma: An unusual presentation

Author

Halder, Chinmay, Sen, Sumit, Gangopadhyay, Anusree, and Bala, Sanchaita

Subjects
Nervous system tumors -- Risk factors -- Diagnosis -- Care and treatment -- Patient outcomes -- Case studies, Health
Abstract

Byline: Chinmay. Halder, Sumit. Sen, Anusree. Gangopadhyay, Sanchaita. Bala Palisaded encapsulated neuroma (PEN) is an infrequent benign cutaneous neural tumor, which usually presents as solitary, asymptomatic, papule or nodule, often [...]

Published
2013

7. Aplasia cutis and ipsilateral congenital melanocytic naevus: An unusual association

Author

Gangopadhyay, Anusree, Ghosh, Arghya, Singha, Joydeep, Halder, Chinmay, and Nag, Falguni

Subjects
Ectodermal dysplasia -- Risk factors -- Diagnosis -- Care and treatment -- Patient outcomes -- Case studies, Health
Abstract

Byline: Anusree. Gangopadhyay, Arghya. Ghosh, Joydeep. Singha, Chinmay. Halder, Falguni. Nag Sir, The term 'aplasia cutis congenita' implies a failure of skin development. The subcutaneous fat may also be partly [...]

Published
2013

8. Leprechaunism - a case report

Author

Sen, Sumit, Roy, Ajitesh, Gangopadhyay, Anusree, and Halder, Chinmay

Subjects
Donohue syndrome -- Diagnosis -- Genetic aspects -- Care and treatment -- Reports, Health
Abstract

Byline: Sumit. Sen, Ajitesh. Roy, Anusree. Gangopadhyay, Chinmay. Halder Sir, Leprechaunism or Donohue's syndrome is a rare condition occurring in less than one in a million births. Marked hypertrichosis, characteristic [...]

Published
2012

9. Granuloma faciale: Exclusively extrafacial

Author

Nag Falguni, Biswas Saugato, Chatterjee Gobinda, Halder Chinmay, Trupti V Surana, and Ghosh Arghyaprasun

Subjects
medicine.medical_specialty, business.industry, Dermatology, lcsh:RL1-803, Dapsone, granuloma faciale, medicine.disease, stomatognathic diseases, Extrafacial, hemic and lymphatic diseases, E-Case Report, polymorphous infiltrate, lcsh:Dermatology, medicine, Granuloma faciale, business, grenz zone, medicine.drug
Abstract

We report a case of granuloma faciale over distal extremities in a 60-year-old man without facial lesions who did not show any response to dapsone.

Published
2013

10. Case Report. Eccrine Angiomatous Hamartoma: Late Onset Facial Presentation.

Author

Halder, Chinmay, Naskar, Biswanath, Biswas, Projna, and Mitra, Pradip K.

Subjects
*TUMOR diagnosis, *HAMARTOMA, *SKIN, *FACIAL anatomy, *CAPILLARIES, *DERMATOLOGY, *SERIAL publications, *SWEAT glands, *ANATOMY, *DIAGNOSIS
Abstract

Eccrine angiomatous hamartoma (EAH) is a very rare benign neoplastic condition characterized by hamartomatous proliferation of eccrine glands and accompanying blood vessels and lymphatics. These lesions are more often present at birth or appear during early infancy and childhood and present as solitary nodule or plaque with occasional pain and sweating. They are generally present on the extremities, mostly the palms and soles. We report here a case of EAH in a 20-year-old female who presented with a solitary angiomatous plaque close to the lower eyelid of the right eye with occasional pain and sweating for its rarity. [ABSTRACT FROM AUTHOR]

Published
2014
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