Search Our Scientific Publications & Authors

Publications
find publications by category +
Translate page:

An Interdisciplinary Management of Avulsed Maxillary Incisors: A Case Report.

Authors:
Revathy Parthasarathy Srividhya Srinivasan Vikram C Yashini Thanikachalam Anupama Ramachandran

Cureus 2022 Apr 6;14(4):e23891. Epub 2022 Apr 6.

Conservative Dentistry and Endodontics, Chettinad Dental College and Research Institute, Chennai, IND.

The current case report presents a case of a road traffic accident comprising dental avulsion of maxillary incisors. A 30-year-old male reported missing teeth following trauma in his upper front tooth region. The avulsion of maxillary right central and lateral incisors along with laceration in upper and lower lips was evident. The avulsed teeth were stored in milk after a brief extra-oral dry time of one hour and were carried to the department with a one-hour delay. After clinical and radiographic investigations, no mobility or fractures were apparently noticed. The avulsed 11 and 12 had closed apices with intact crown and root surfaces. Following an extra-oral endodontic therapy, immediate replantation was scheduled. Subsequently, the alveolar sockets were irrigated with saline to dislodge the clot and any gross debris that was present. Teeth were reimplanted into the socket after placement of PRF membrane around the root surface. A semi-rigid wire and composite splinting were done for a span of two weeks and antibiotics were prescribed. An exploratory CBCT taken revealed a cortical bone loss in the buccal region of 12 and 11. An interdisciplinary approach to regenerate the osseous defect was then carried out. A follow-up of two weeks, four weeks, three months, six months, and a year was done. Evaluation performed after a year revealed the absence of clinical symptoms and satisfactory healing with no signs of resorption radiographically.

Download full-text PDF

 Source
http://dx.doi.org/10.7759/cureus.23891DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9075823PMC
April 2022

Publication Analysis

Top Keywords

case report
8
maxillary incisors
8
avulsion maxillary
8
resorption radiographically
4
alveolar sockets
4
sockets irrigated
4
irrigated saline
4
saline dislodge
4
dislodge clot
4
clot gross
4
gross debris
4
debris teeth
4
scheduled subsequently
4
teeth reimplanted
4
reimplanted socket
4
socket placement
4
placement prf
4
prf membrane
4
membrane root
4
root surface
4

Keyword Occurance

Similar Publications

Custom-made 3D-printed porous metal acetabular composite component in revision hip arthroplasty with Paprosky type III acetabular defects: A case report.

Authors:
Cong Xiao Shaoyun Zhang Zhixiang Gao Chongqi Tu

Technol Health Care 2022 Jul 29. Epub 2022 Jul 29.

Department of Orthopedics, West China Hospital, Sichuan University, Chengdu, Sichuan, China.

Background: Increases in the numbers of surgical procedures for primary total hip arthroplasty (THA) inevitably lead to increases in the requirements for revision THA. The achievement of long-term stability is difficult or impossible by conventional implants in patients with severe destruction of the acetabulum.

Objective: This case report presents a successful treatment using a specific three-dimensional (3D)-printed porous titanium acetabular composite component without a flange in the management of Paprosky type IIIB acetabular defects. Read More

View Article and Full-Text PDF
July 2022
Similar Publications

Unusual Case of Mirizzi Syndrome Presenting as Painless Jaundice.

Authors:
Justin Bauzon Sarah Haller Jose R Aponte-Pieras Daisy Lankarani Ariyon Schreiber Nazanin Houshmand Shahid Wahid

Am J Case Rep 2022 Aug 14;23:e936836. Epub 2022 Aug 14.

Department of Internal Medicine, Division of Gastroenterology and Hepatology, Kirk Kerkorian School of Medicine at University of Nevada Las Vegas, Las Vegas, NV, USA.

BACKGROUND Isolated painless jaundice is an uncommon presenting sign for Mirizzi syndrome, which is typically characterized by symptoms of acute or chronic cholecystitis. We report a rare case of Mirizzi syndrome with an acute onset of painless obstructive jaundice. CASE REPORT A 60-year-old man with an unremarkable prior medical history presented with 1 week of jaundice, dark urine, and acholic stools. Read More

View Article and Full-Text PDF
August 2022
Similar Publications

Short stature and melanocytic nevi in a girl with ARID1B-related Coffin-Siris syndrome: a case report.

Authors:
Dong-Ying Tao Huan-Hong Niu Jing-Jing Zhang Hui-Qin Zhang Ming-Hua Zeng Sheng-Quan Cheng

BMC Pediatr 2022 Aug 13;22(1):486. Epub 2022 Aug 13.

Department of Pediatrics, Xijing Hospital, Fourth Military Medical University, No. 127 Changle West Road, Xincheng District, Xi'an, 710032, Shaanxi Province, China.

Background: Coffin-Siris syndrome (CSS) is a rare autosomal dominant disorder characterized by intellectual disability, developmental delay, and characteristic facial features. Few patients with cutaneous phenotype in this rare syndrome have been reported.

Case Presentation: Herein, we describe a 12-year-old Chinese girl diagnosed with CSS, who was referred to our hospital because of intellectual disability and short stature. Read More

View Article and Full-Text PDF
August 2022
Similar Publications

Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis.

Authors:
Gregorio Serra Luigi Memo Paola Cavicchioli Mario Cutrone Mario Giuffrè Maria Laura La Torre Ingrid Anne Mandy Schierz Giovanni Corsello

Ital J Pediatr 2022 Aug 13;48(1):145. Epub 2022 Aug 13.

Department of Health Promotion, Mother and Child Care, Internal Medicine and Medical Specialties "G. D'Alessandro", University of Palermo, Palermo, Italy.

Background: Congenital ichthyosis (CI) is a heterogeneous group of genetic disorders characterized by generalized dry skin, scaling and hyperkeratosis, often associated to erythroderma. They are rare diseases, with overall incidence of 6.7 in 100,000. Read More

View Article and Full-Text PDF
August 2022
Similar Publications

Unexpectedly rapid decrease in the size of a spinal epidural abscess after percutaneous posterior pedicle screw fixation without decompression surgery: a case report.

Authors:
Go Kubota Yasuchika Aoki Yusuke Sato Masashi Sato Satoshi Yoh Takayuki Nakajima Masahiro Inoue Hiroshi Takahashi Arata Nakajima Yawara Eguchi Sumihisa Orita Koichi Nakagawa Seiji Ohtori

Spinal Cord Ser Cases 2022 Aug 13;8(1):77. Epub 2022 Aug 13.

Department of Orthopaedic Surgery, Graduate School of Medicine, Chiba University, Chiba-city, Chiba, Japan.

Introduction: Spondylodiscitis accompanying spinal epidural abscess is often treated with decompression surgery when there are neurological symptoms. We report a case of spondylodiscitis accompanying spinal epidural abscess with severe lower extremity pain that was successfully treated with percutaneous posterior pedicle screw fixation without decompression surgery.

Case Presentation: A 53-year-old man was admitted to our hospital with severe low back pain (LBP), lower extremity pain and numbness, and fever. Read More

View Article and Full-Text PDF
August 2022
Similar Publications
}