Rashmi Agarwal

University College of Medical Sciences

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Hemant Gupta

Babu Banarasi Das University

Hemant Mehra

Babu Banarasi Das University

BS Chandrashekar

Indian Academy of Sciences

Subhra Dhar

Institute of Child Health

Sahana M. Srinivas

Indira Gandhi Institute of Child Health

Sandipan Dhar

University of Kentucky

Meenal Tepan

Bharati Vidyapeeth Deemed University

Subodh Shankar Natu

Integral University

Kurt R. Weiss

University of Pittsburgh

Abhigyan Kumar

Cancer Institute (WIA)

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Creative Commons

Washington University in St. Louis

Bharati Vidyapeeth Deemed University

Babu Banarasi Das University

Guru Teg Bahadur Hospital

University of Pittsburgh

Amrita Institute of Medical Sciences and Research Centre

Indian Academy of Sciences

University College of Medical Sciences

EduInnovation

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An Atypical Presentation of Multiple Central Osteomas Mimicking Craniofacial Fibrous Dysplasia – A Pictorial Essay

JOURNAL OF CLINICAL AND DIAGNOSTIC RESEARCH (2016)

Rashmi Agarwal Amit Mhapuskar Manjula Hebbale Meenal Tepan Ayushee

Osteoma is benign neoplasm with slow growth characterized by deposition of compact lamellar cortical or cancellous bone creating a tumour mass. It is still unclear whether osteomas are benign neoplasms or hamartomas. They have typical clinical presentations and are easily diagnosed with the help of radiographs. We present a rare case of non-syndromic multiple osteomas in the craniofacial region which are typically restricted to the midline and presents radiographically as craniofacial fibrous dysplasia causing a diagnostic dilemma.

Osteoma

Presentation (obstetrics)

10.7860/jcdr/2016/21350.8806

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A rare case of unilateral acral speckled hypopigmentation

International Journal of Dermatology (2021)

Hania Qamar Khan Sahana M. Srinivas Rashmi Agarwal Subhra Dhar

Hypopigmentation

Child Health

10.1111/ijd.16020

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Assessment of Intraoperative Blood Loss During Oral and Maxillofacial Surgical Procedures and its Implications

Journal of Maxillofacial and Oral Surgery (2021)

Ishita Srivastava Hemant Gupta Rashmi Agarwal Hemant Mehra A.K. Gangwar

10.1007/s12663-021-01663-5

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Application of calcium sulfate as graft material in implantology and maxillofacial procedures: A review of literature

National Journal of Maxillofacial Surgery (2024)

Hemant Gupta Ashish Pandey Rashmi Agarwal Hemant Mehra Swati Gupta

Calcium sulphate (plaster of Paris) has been used since 1892 to fill bone defects and as a good bone graft substitute. Calcium sulphate is an osteoconductive, inorganic substance. Following 75 years, many other authors reported variable and a better result in grafting of bone defects and in several cases of immediate and delayed dental implants for good osseointegrations, with no complications attributed to the calcium sulphate. Early results were variable, because of its conflicting crystalline structure, purity, and quality of the calcium sulphate. Apart from this, calcium sulphate also shows predictable resorption rate in vivo , presence of minimal trace elements and extremely uniform crystalline structure. Calcium sulphate is a bio-inert material and get resorbed over a period of weeks and fibrovascular tissue takes its place which eventually allows neovascularization and bone formation within the area. Use During the conventional surgical treatment addition of calcium sulphate as a bone graft of in case of placement of dental implants and pathological bony defects it improves the clinical outcome. Calcium sulphate also act as a barrier and filling material for the treatment of “through and through” bony lesions. Use of calcium sulphate as a bone graft substitute avoids the complications and morbidity associated with autograft like infection, second surgery.

10.4103/njms.njms_33_22

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Overnight alopecia: A subtype of acute diffuse and total alopecia?

International Journal of Trichology (2019)

Rashmi Agarwal BS Chandrashekar Chaithra Shenoy

Acute diffuse and total alopecia (ADTA) is a variant of alopecia areata which lacks the typical patchy hair loss seen in classical alopecia areata and presents with an acute onset of diffuse hair loss commonly reported in young females with the duration from disease onset to diffuse hair loss ranging from 2 to 20 weeks. Although the clinical features of ADTA resemble telogen effluvium, dermoscopy can prove to be a useful tool for differentiating these two conditions and avoiding unnecessary investigations as specific dermoscopic findings of alopecia areata are invariably present along the disease course. Herein, we report a case of ADTA in a 42-year-old Indian female who presented with sudden onset of diffuse hair loss of only 1-day duration.

10.4103/ijt.ijt_36_19

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Co-occurrence of tuberous sclerosis with port wine stain

Indian Journal of Paediatric Dermatology (2021)

Rashmi Agarwal S Suganya BS Chandrashekar Sahana M. Srinivas

Tuberous sclerosis complex is a rare autosomal dominant neurocutaneous disorder characterized by the presence of multiple tumors influencing diverse body frameworks including the central nervous system, skin, eyes, heart, lungs, kidney, and bones. It is described by cutaneous changes, neurologic conditions, and the presence of hamartomas in numerous organs. The treatment of these patients requires a multidisciplinary approach. A port-wine stain is characterized as a telangiectatic macule that manifests during childbirth and stays all throughout life. They are associated with many syndromes. This article reports a rare case of co-occurrence of tuberous sclerosis with port-wine stain in a 2-year-old baby.

Port-wine stain

10.4103/ijpd.ijpd_179_20

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