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Featured researches published by D.O Awange.


Journal of Craniofacial Surgery | 2008

Clinicopathologic features of ameloblastoma in Kenya: a 10-year audit.

Vilembwa L. Adeline; Elizabeth Dimba; Ka Wakoli; Anthony Njiru; D.O Awange; John F. Onyango; Ml Chindia

This study describes the clinical and pathologic features of ameloblastomas seen in the 2 main craniofacial treatment centers in Kenya in the 10-year period between January 1995 and December 2005. A total of 184 patient records were analyzed for this study. Eighty-two (44.6%) of the patients were male, and 102 (55.4%) were female with an overall age range of 10 to 80 years (mean, 30.2 years; SD, 14.1 years). There was no significant difference in gender presentation of ameloblastomas, although females presented at a slightly older age. The mean age for males was 29.9 years, and for females, it was 30.5 years. Patients generally tended to seek medical advice late, with the mean duration at first presentation of 46.3 months for males and 44.4 months for females. Most of the ameloblastomas (n = 172; 93.5%) were located in the mandible, 11 (6.0%) were in the maxilla, and 1 (0.5%) was in the soft tissues. Presenting symptoms included swelling (n = 182; 98.9%), pain (n = 64; 36.0%), mobile teeth/history of extraction (n = 104; 57.5%), purulent discharge (n = 39; 21.7%) and paresthesia (n = 10; 5.6%). The posterior mandible was the most commonly affected site, whereas maxillary ameloblastomas tended to occur in anterior sites. One hundred fifty-three ameloblastomas (83.2%) were of the solid/multicystic subtype; 8 (5.3%) were unicystic; 1 (0.5%) was of extraosseous origin; 1 (0.5%) was desmoplastic; 9 (6.0%) were malignant, and 12 of the records had no histopathologic pattern specified.


British Dental Journal | 1994

CONGENITAL EPULIS OF THE NEWBORN : A REPORT OF TWO CASES

Ml Chindia; D.O Awange

Congenital epulis of the newborn is a rare lesion whose histogenesis and natural clinical history have remained obscure. Even with the advent of modern histopathological techniques, it has not been possible to depict specific cellular features unique to this lesion. However, it is important that new cases are reported from all populations so that their occurrence and frequency may be easily noted. Furthermore, the lesion is important as a differential diagnosis of other aggressive lesions early in life. This report presents two Kenyan cases


Journal of Cranio-maxillofacial Surgery | 2013

keratocystic odontogenic tumours of the jaws and associated pathologies - a 10 year clinicopathologic audit in a referral teaching hospital in kenya

Benjamin N. Simiyu; Fawzia Butt; Elizabeth Dimba; Wagaiyu Eg; D.O Awange; Symon W. Guthua; Pieter J. Slootweg

AIM To establish the pattern of occurrence and the clinicopathological features of keratocystic odontogenic tumour (KCOT) over a 10-year period. MATERIALS AND METHOD Patients from the University of Nairobi Dental Hospital treated for KCOT were included in the study over a 10-year period. The study highlights the demographic, clinico-radiological and histological features of these tumours. RESULTS A total of 22 confirmed cases of KCOTs were recorded with equal gender prevalence; (M:F = 1.44:1). The age range of the patients was from 10 to 69 years with a peak in the second decade of life (mean = 27.5 yrs). Of the 22 cases, 15 (68.2%) occurred in the mandible of which eight (53.3%) involved the body, five (33.4%) the angle and ramus. Six (27.3%) occurred in the maxilla, and one (4.5%) was in both jaws and was associated with Gorlin-Goltz Syndrome. The most common presenting complaint in most patients was swelling 54.6%, and in 18.2% was incidental finding. Eight (36.4%) cases showed satellite cysts upon pathologic evaluation. Thirteen (59.1%) cases were managed by surgical excision, while nine (40.9%) were managed by enucleation. CONCLUSION Based on the outcome of this study, KCOT present mostly in body, angle and ramus of the mandible and its peak is in the second decade of life.


Journal of Cranio-maxillofacial Surgery | 1998

Osteosarcoma of the maxillofacial bones in Kenyans

Ml Chindia; Symon W. Guthua; D.O Awange; Ka Wakoli

Osteosarcoma (OS) is a highly malignant tumour and is the most common primary neoplasm of bone; although rare, especially in the maxillofacial skeleton. This article presents 14 Kenyan cases of OS of the maxillofacial bones seen between January 1991 and July 1997: 11 in the mandible, two in the maxilla and one in the right zygomatic arch. Patients ranged in age from one week to 50 years (Mean = 29.7), with an equal gender distribution. While pain and rapid swelling were the commonest clinical features, the radiographic and histopathological characteristics were as varied as has been described elsewhere. Generally, effective management of most of the cases was poor due to late presentation for treatment.


International Journal of Prosthodontics | 2004

Maxillary obturator prosthesis rehabilitation following maxillectomy for ameloblastoma: case series of five patients.

B.I. Omondi; Symon W. Guthua; D.O Awange; Walter Odhiambo


International Dental Journal | 2007

An audit of oral diseases at a Nairobi centre, 2000-2004

Elizabeth Dimba; J. Gichana; Ak Limo; Ka Wakoli; Ml Chindia; D.O Awange


East African Medical Journal | 1993

Oral verrucous carcinoma : report of two cases and review of literature

D.O Awange; Onyango Jf


East African Medical Journal | 1995

Oral tumours and tumour-like conditions in Kenya: II. Age, sex and site distribution.

Onyango Jf; D.O Awange; Wakiaga Jm


East African Medical Journal | 1992

Salivary gland tumours in Kenya

Onyango Jf; D.O Awange; J. M. Muthamia; B. I. O. Muga


East African Medical Journal | 2009

REACTIVE LOCALISED INFLAMMATORY HYPERPLASIA OF THE ORAL MUCOSA

D.O Awange; Ka Wakoli; Onyango Jf; Ml Chindia; Eo Dimba; Symon W. Guthua

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Ka Wakoli

University of Nairobi

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Wakiaga Jm

University of Manchester

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Mk Akama

University of Nairobi

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David Mwaniki

Kenya Medical Research Institute

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