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Habitual khat chewing and oral melanoacanthoma: A case report 被引量:1
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作者 Hamad Albagieh Ashwag Aloyouny +5 位作者 Rana Alshagroud Abdulaziz Alwakeel Shahad Alkait Fatimah Almufarji Ghadeer Almutairi Rana Alkhalaf 《World Journal of Clinical Cases》 SCIE 2023年第2期449-455,共7页
BACKGROUND Habitual khat(Catha edulis) chewing has been proven to cause numerous oral tissue changes. However, oral melanoacanthoma triggered by chronic khat chewing is rare. Oral melanoacanthoma is an uncommon, sudde... BACKGROUND Habitual khat(Catha edulis) chewing has been proven to cause numerous oral tissue changes. However, oral melanoacanthoma triggered by chronic khat chewing is rare. Oral melanoacanthoma is an uncommon, sudden, asymptomatic, benign pigmentation of the oral cavity. Under the microscope, the epithelial layer of the oral mucosa showed dendritic melanocyte proliferation and acanthosis. The study aimed to highlight chronic khat chewing as a trigger for oral melanoacanthoma.CASE SUMMARY In the current study, we report a case of a 26-year-old male patient with a rare presentation of oral melanoacanthoma triggered by regular khat chewing. Many intrinsic and extrinsic factors can cause oral pigmentation. Chewing khat is an extrinsic factor that can cause several diseases, including oral pigmentation. In this case, the definitive diagnosis was oral melanoacanthoma. This diagnosis was made based on the patient’s history, clinical lesion presentation, and microscopic biopsy results.CONCLUSION Habitual khat(Catha edulis) chewing causes many oral tissue changes including oral melanoacanthoma. The study aimed to highlight chronic khat chewing as a trigger for oral melanoacanthoma. 展开更多
关键词 oral melanoacanthoma oral lesion Qaat chewing oral pigmentation Brown pigmentation Benign lesion Case report
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Laugier-Hunziker syndrome:a report of three cases and literature review 被引量:5
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作者 Wen-Mei Wang Xiang Wang +2 位作者 Ning Duan Hong-Liu Jiang Xiao-Feng Huang 《International Journal of Oral Science》 SCIE CAS CSCD 2012年第4期226-230,共5页
Laugier-Hunziker syndrome (LHS) is an acquired pigmentary condition affecting lips, oral mucosa and acral area, frequently associated with longitudinal melanonychia. There is neither malignant predisposition nor und... Laugier-Hunziker syndrome (LHS) is an acquired pigmentary condition affecting lips, oral mucosa and acral area, frequently associated with longitudinal melanonychia. There is neither malignant predisposition nor underlying systemic abnormality associated with LHS. Herein, we present three uncommon cases of LHS with possibly new feature of nail pigmentation, which were diagnosed during the past 2 years. We also review the clinical and histological findings, differential diagnosis, and treatment of the syndrome in published literature. 展开更多
关键词 differential diagnosis Laugier-Hunziker syndrome longitudinal melanonychia oral pigmentation
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