scholarly journals Ectopic maxillary tooth as a cause of recurrent maxillary sinusitis: a case report and review of the literature

2020 ◽  
Vol 2020 (9) ◽  
Author(s):  
Ali Almomen ◽  
B Alkhudair ◽  
A Alkhatib ◽  
G Alazzah ◽  
Zainab Ali ◽  
...  
Keyword(s):  
Case Report ◽  
Maxillary Sinusitis ◽  
Third Molar ◽  
Young Male ◽  
Endoscopic Management ◽  
Rare Presentation ◽  
Maxillary Tooth ◽  
Dentigerous Cysts ◽  
Rare Case Report ◽  
Ectopic Tooth

Abstract This article presents a rare case report of an ectopic third molar tooth located in the medial wall of maxillary sinus in a young male manifesting as recurrent sinusitis along with upper jaw pain and postnasal discharge diagnosed with an ectopic tooth and bilateral dentigerous cysts. This article aims to discuss this rare presentation of an ectopic tooth as a cause of recurrent maxillary sinusitis and the endonasal endoscopic management of the case.

Frontal mucocele caused by an ectopic maxillary tooth

2007 ◽  
Vol 122 (12) ◽  
pp. 1384-1385 ◽  
Author(s):  
M A Buchanan ◽  
S E Prince ◽  
P R Prinsley
Keyword(s):  
Computed Tomography ◽  
Case Report ◽  
Endoscopic Sinus Surgery ◽  
Conventional Treatment ◽  
Maxillary Sinusitis ◽  
Signs And Symptoms ◽  
Sinus Surgery ◽  
Documented Case ◽  
Maxillary Tooth ◽  
Ectopic Tooth

AbstractObjective:To present a previously unreported cause of frontal mucocele.Case report:A patient presented with a frontal mucocele and maxillary sinusitis. Computed tomography revealed an ectopic maxillary tooth as the cause of her signs and symptoms. Removal of the tooth by a Caldwell–Luc procedure facilitated resolution of the mucocele. Conventional treatment of mucoceles by endoscopic sinus surgery, and other rhinological sequelae of ectopic teeth, are considered.Conclusion:This is the first documented case of an ectopic tooth causing a frontal mucocele, and demonstrates how effectively the patient's symptoms resolved on removal of the tooth.

scholarly journals Syphilitic Balanitis of Follmann, A Rare Case Report

2021 ◽  
Vol 19 (1) ◽  
pp. 71-73
Author(s):  
Pooja Agarwal ◽  
Ashish Jagati ◽  
Priyanka Vadher ◽  
Malay Chaudhary
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Rare Presentation ◽  
Heterosexual Male ◽  
Primary Syphilis ◽  
Rare Case Report

Syphilitic balanitis of Follmann is a rare presentation of primary syphilis. It can occur before or after the appearance of primary chancre and some time without any associated primary chancre. We are reporting a case of syphilitic balanitis of Follmann, in a 23 years old heterosexual male, who presented with balanitis associated with single indurated lesion over coronal sulcus and few superficial ulcers over prepuce.

scholarly journals Psoriasiform Mycosis Fungoides Involving the Face- A Rare Case Report

2021 ◽  
pp. 94-99
Author(s):  
N. R. Vignesh ◽  
Shreya Srinivasan ◽  
G. Sukanya ◽  
S. Arun Karthikeyan
Keyword(s):  
Case Report ◽  
Mycosis Fungoides ◽  
Rare Case ◽  
Cell Lymphoma ◽  
Punch Biopsy ◽  
Cutaneous T Cell Lymphoma ◽  
Rare Presentation ◽  
Rare Case Report ◽  
Atypical Cells ◽  
The Face

Mycosis fungoides is represented as the most common epidermotropic cutaneous T-cell lymphoma, which is mainly characterized by the proliferation of atypical cells within the epidermis. We report a rare presentation of mycosis fungoides in a 60-year-old male presenting with chronic psoriasiform plaque involving the face. Punch biopsy of the lesion from the forehead was taken for routine histological examination and immunohistochemical stains. Results of biopsy and immunohistochemical findings were consistent with mycosis fungoides and diagnosed as psoriasiform presentation of mycosis fungoides involving the face.

scholarly journals Lipoma in Penis : A Rare Case Report

2013 ◽  
Vol 3 (1) ◽  
pp. 24-25
Author(s):  
T Ahmed ◽  
MA Kalam ◽  
II Mannan ◽  
MA Simi
Keyword(s):  
Case Report ◽  
Plastic Surgery ◽  
Male Patient ◽  
Rare Case ◽  
Young Male ◽  
Histopathological Analysis ◽  
Review Of The Literature ◽  
Ventral Aspect ◽  
Rare Case Report ◽  
Pedunculated Tumor

In this article we report one case of lipoma of the penis in a twenty three years old young male. This site of lipoma is rare. A case of a young male patient who consulted for removal of a penile lump is presented. The small, regular, wellcircumscribed pedunculated tumor localized on the ventral aspect of the penis was excised. The histopathological analysis showed a benign lipoma. A review of the literature showed lipoma of the penis to be very uncommon. For this reason, we were prompted to report this case.DOI: http://dx.doi.org/10.3329/bdjps.v3i1.15003 Bangladesh Journal of Plastic Surgery 2012, 3(1): 24-25

scholarly journals Multiple Extramedullary Plasmacytoma with Lytic Bony Lesions: A Rare Case Report

2013 ◽  
Vol 2013 ◽  
pp. 1-3 ◽  
Author(s):  
Akhlak Hussain ◽  
Mohinder Singh ◽  
Kuldip Singh ◽  
Harjot Bagga
Keyword(s):  
Bone Marrow ◽  
Case Report ◽  
Soft Tissue ◽  
Subcutaneous Tissue ◽  
Extramedullary Plasmacytoma ◽  
Rare Presentation ◽  
Multiple Organs ◽  
Lytic Lesions ◽  
Rare Case Report ◽  
Bony Lesions

Objective. Multiple extramedullary plasmacytoma lesions involving subcutaneous tissue, breast, mediastinal tissue, spleen, and soft tissue of pelvic region along with multiple bones plasmacytomas without marrow plasmacytosis are a very rare presentation.Design. Case report.Result. A 54-year-old female was found to have multiple small bony lytic lesions, multiple extramedullary soft tissue plasmacytomas, serum M protein >3 g/dL, and elevated ESR. Bone marrow aspirate did not reveal any evidence of multiple myeloma/plasmacytosis. There was no anemia, hypercalcemia, or renal insufficiency.Conclusion. Extramedullary plasmacytoma can involve multiple organs at a time including bones and soft tissue without involving bone marrow.

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