scholarly journals Pigmented Fungiform Papillae of the Tongue and Lingual Fimbriae as Single Presentation in Adult: A Case Report and Literature Review

2020 ◽  
Vol 14 (04) ◽  
pp. 702-706
Author(s):  
Meircurius Dwi Condro Surboyo ◽  
Diah Savitri Ernawati ◽  
Adiastuti Endah Parmadiati ◽  
Riyan Iman Marsetyo
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Oral Mucosa ◽  
Clinical Examination ◽  
Pathological Condition ◽  
Systemic Disease ◽  
Specific Treatment ◽  
Ventral Surface ◽  
Fungiform Papillae ◽  
Single Presentation

AbstractThe normal variant in the oral mucosa is a nonpathological condition. Clinical examination must be carefully performed to avoid misdiagnosis as pathological condition. We reported two rare cases of pigmented fungiform papillae and lingual fimbria. Case 1 presented a 22-year-old Javanese man, with no systemic disease and several dark patches over the tongue for2 years. Case 2 presented a 21-year-old Javanese woman with dark patches over the dorsal and lateral of the tongue which had been known for over 4 to 5 months. Both patients had no systemic issues and there were no complaints about the patches. The dark patches, which appeared in both cases, were found together with linear small bumps on the ventral surface of the tongue and near the lingual frenulum. Further examination and specific treatment were not carried out, in accordance with the condition on the tongue.

Oral collision cancer: A case report and literature review of simultaneous squamous cell and adenoid cystic carcinoma of the oral mucosa

2021 ◽  
Author(s):  
Satoru Ogane ◽  
Takamasa Kawano ◽  
Chiho Hiraga (Kondo) ◽  
Taiki Suzuki ◽  
Kazuhiko Hashimoto ◽  
...  
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Adenoid Cystic Carcinoma ◽  
Oral Mucosa ◽  
Squamous Cell ◽  
Adenoid Cystic

scholarly journals Imatinib-related hyperpigmentation of oral mucosa: Case report and literature review

2019 ◽  
Vol 14 (3) ◽  
pp. 335-337 ◽  
Author(s):  
Marco Mascitti ◽  
Elisa Luconi ◽  
Lucrezia Togni ◽  
Alberta Barlattani ◽  
Andrea Santarelli
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Oral Mucosa

scholarly journals Metastasis from Penile Squamous Cell Carcinoma to Brain: A Case Report and Review of Literature

2017 ◽  
Vol 07 (02) ◽  
pp. 164-167
Author(s):  
Hanish Bansal ◽  
Ashwani Chaudhary ◽  
Dipesh Batra ◽  
Rohit Jindal
Keyword(s):  
Squamous Cell Carcinoma ◽  
Case Report ◽  
Brain Metastasis ◽  
Literature Review ◽  
Rare Case ◽  
Systemic Disease ◽  
Penile Carcinoma ◽  
Review Of Literature ◽  
Penile Squamous Cell Carcinoma

AbstractWe report a very rare case of a 63-year-old man with penile carcinoma who developed brain metastasis. Brain metastasis from penile carcinoma is very rare, and only six cases have been reported so far as per our literature review. In view of controlled primary tumor and absence of systemic disease, tumor was excised and the patient remained clinically controlled till 3 months after follow-up.

Elastofibromatous change of the oral mucosa: case report and literature review

2010 ◽  
Vol 37 (10) ◽  
pp. 1067-1071 ◽  
Author(s):  
Cassiano Francisco Weege Nonaka ◽  
Delane Maria Rêgo ◽  
Márcia Cristina da Costa Miguel ◽  
Lélia Batista De Souza ◽  
Leão Pereira Pinto
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Oral Mucosa

scholarly journals Geographic Stomatitis with Multiple Areas Involvement of Oral Cavity: A Case Report and Review of Literatures

2021 ◽  
Vol 10 ◽  
pp. 2107
Author(s):  
Farid Abbasi ◽  
Aliyeh Sehatpour ◽  
Seyed Masoud Sajedi ◽  
Parisa Bahadori ◽  
Mohadeseh Nouri
Keyword(s):  
Case Report ◽  
Oral Cavity ◽  
Oral Mucosa ◽  
Benign Lesion ◽  
Ventral Surface ◽  
Unknown Etiology ◽  
Clinical Appearance ◽  
Clinicopathologic Findings ◽  
Characteristic Features ◽  
Rule Out

Background: Geographic stomatitis is an uncommon migratory benign lesion of oral mucosa with unknown etiology. It can affect all the areas of the oral mucosa, but the dorsum and lateral borders of the tongue are the most commonly involved areas called geographic tongue. The clinical appearance of this condition is the oval or circular erythematous areas with irregular elevated keratotic borders. These characteristic features of geographic stomatitis are diagnostic for all clinicians when appearing on the dorsum of the tongue, despite other affected areas of oral mucosa that can confuse clinicians. This condition may be associated with some diseases such as psoriasis, Reiter’s syndrome, and atopic conditions, so the clinicians should rule out these diseases and diagnose the geographic stomatitis. Case Report: A 17-year-old male attended to our department for a routine dentistry checkup. During the intraoral examination, we found multiple erythematous areas surrounded by a thin white border on different surfaces of his oral cavity. His extraoral examinations were completely normal. Conclusion: Due to the rarity of this lesion on the other sites of oral mucosa rather than dorsum and lateral borders of the tongue such as labial mucosa, buccal mucosa, the floor of the mouth, ventral surface of the tongue, and palate, it is necessary to report, study and evaluate each case of this condition that clinicopathologic findings have confirmed this diagnosis, to treat and advice these patients on the best approach. [GMJ.2021;10:e2071]

scholarly journals Unilateral Renal Cystic Disease: A Case Report and Literature Review

2020 ◽  
Vol 8 (C) ◽  
pp. 160-163
Author(s):  
Darmadi Darmadi ◽  
Riska Habriel Ruslie ◽  
Nurlaila Qodrianti Siregar ◽  
Deli Theo ◽  
Syahrial Anas
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Specific Treatment ◽  
Family Health ◽  
Cystic Disease ◽  
Renal Cystic Disease ◽  
Health Related ◽  
Unilateral Renal Cystic Disease ◽  
Laboratory Examinations

BACKGROUND: URCD is a rare disease characterized by cysts with various sizes in a diffusely enlarged kidney without forming a distinct encapsulated mass. We present literature review and report a case of URCD in our center. The aim of the study was to report a case of unilateral renal cystic disease (URCD) in a 25-year-old female. CASE REPORT: The patient was a 25-year-old female. She came to emergency unit of Mitra Medika Amplas Hospital Medan, Indonesia, with dyspepsia associated symptoms. Physical examination and family health-related history were normal. Laboratory examinations and genetic evaluation showed no abnormalities. Ultrasonography examination revealed multiple cysts in her right kidney which was confirmed by computed tomography (CT) scan. The diagnosis of URCD was confirmed. No specific treatment was given and she was advised to do a routine follow-up. CONCLUSION: URCD may present with mild symptoms or even asymptomatic. Diagnosis is confirmed by imaging modalities with normal renal function and absence of genetic predisposition. The management is conservative. Routine follow-up is mandatory.

scholarly journals Multiple pilomatrixomas: Case report and literature review

2008 ◽  
Vol 87 (4) ◽  
pp. 230-233 ◽  
Author(s):  
Shashidhar Sadda Reddy ◽  
Swarupa A. Gadre ◽  
Patrick Adegboyega ◽  
Arun K. Gadre
Keyword(s):  
Differential Diagnosis ◽  
Case Report ◽  
Literature Review ◽  
Lymph Nodes ◽  
Black Woman ◽  
Clinical Examination ◽  
Surgical Excision ◽  
Hair Matrix ◽  
The Masses ◽  
Epithelial Neoplasm

Pilomatrixoma is a rare, benign, circumscribed, calcifying epithelial neoplasm that is derived from hair matrix cells. Multiple pilomatrixomas are uncommon. We describe a case of multiple pilomatrixomas in a 23-year-old black woman who presented with lesions on her face and back. Based on the results of the clinical examination, she was provisionally diagnosed with either calcified sebaceous cysts or calcified lymph nodes. She underwent surgical excision of the masses. On histopathology, the lesions were identified as pilomatrixomas. We attribute our original failure to diagnose this condition to our lack of familiarity with it. We discuss the presentation, differential diagnosis, and other characteristics of pilomatrixomas.

scholarly journals Keloid Formation after Circumcision: A Case Report and Current Literature Review

Folia Medica ◽  
2020 ◽  
Vol 62 (3) ◽  
pp. 601-604
Author(s):  
Yavuz Guler ◽  
Akif Erbin ◽  
Gokhun Ozmerdiven
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Current Literature ◽  
Topical Steroid ◽  
Ventral Surface ◽  
Early Postoperative Period ◽  
Intralesional Injection ◽  
Keloid Formation ◽  
Silicone Gel Sheet

Although penile keloid formation can be seen after major penile surgeries, it is rarely reported after circumcision and there is no standard method for the treatment of this complication. We present a patient who was admitted with a penile keloid mass that occurred after circumcision surgery and discuss the treatment we administered in light of the current literature review. A 7-year-old white boy was admitted to our clinic with a swollen stiff mass on the foreskin six months after circumcision. The parents indicated that no complication occurred in the early postoperative period. Physical examination revealed a white-colored stiff mass measuring approximately 2×1.5 cm in size along the penile ventral surface. Intralesional injection of 0.5 ml triamcinolone acetonide was administered for 12 weeks. At 9 months after circumcision, the keloid tissue was resected. Beginning from the first postoperative week, a silicone gel sheet and topical steroid application were administered for 8 weeks. At a 1-year follow-up, the penis had a satisfactory appearance.

scholarly journals Labial vitiligo associated with a factice disorder: a case report

2018 ◽  
Vol 24 (4) ◽  
pp. 167-169
Author(s):  
Margaux Fricain ◽  
Pierre Weidmann ◽  
Yvon Roche ◽  
Jean Christophe Fricain
Keyword(s):  
Folic Acid ◽  
Case Report ◽  
Vitamin C ◽  
Oral Mucosa ◽  
Clinical Examination ◽  
North Africa ◽  
Skin Involvement ◽  
Upper Lip ◽  
Immune Disease ◽  
Sharp Edges

Introduction: Vitiligo is a non-contagious leukoderma. The loss of melanocytes result in a local hypopigmentation like white symmetrical plaques with sharp edges, most of the time surrounded by hyperpigmentation. It might be an auto immune disease with a genetic predisposition linked to psychological disorders. Oral mucosa vitiligo has rarely been described in the literature. Observation: A seventeen years old patient, native from North Africa, has consulted for a half left upper lip depigmentation appeared in October 2016. The dermatologist had made the diagnosis of vitiligo and prescribed vitamin C and folic acid, without any result. In July 2017, as the lesion has extended to the whole upper lip, the patient came to oral mucosa pathology consultation. Anamnesis revealed a chronic lips chewing. Clinical examination revealed a linear vermillion border depigmentation of the upper lip associated with peripheral pigment enhancement, as well as digital cutaneous involvement. The prescribed treatment was: tacrolimus 0.1% twice daily in local application, stopping practice disorder and sun protection. Comment: Diagnosis of vitiligo is based on clinical examination that can differentiate a segmental vitiligo (localized on at least one dermatomes) of a non-segmental vitiligo (acrofacial, generalized, universalis). Vitiligo of the oral mucosa is rare. It has mainly been described in India. Oral mucosa involvement would affect 55% of patient and the lip would be affected in almost one in two cases in this population. Conclusion: Oral mucosa vitiligo must be known by oral surgeon who has to master the diagnosis and treatments in association with dermatologist, given the concomitant skin involvement that is almost mandatory.

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