scholarly journals Multiple sialolithiasis in submandibular gland duct: a rare case report

2020 ◽  
Vol 68 ◽  
Author(s):  
João Batista da SILVEIRA JUNIOR ◽  
Joaquim Barbosa MATIAS NETO ◽  
Ildeu ANDRADE JUNIOR ◽  
Herminia Marques CAPISTRANO
Keyword(s):  
Case Report ◽  
Salivary Glands ◽  
Submandibular Gland ◽  
Female Patient ◽  
Rare Case ◽  
Surgical Intervention ◽  
Pathological Process ◽  
Floor Of Mouth ◽  
Rare Case Report ◽  
Gland Duct

ABSTRACT Sialolithiasis is a pathological process that affects the major salivary glands. It consists of calcifications that obstruct the parenchyma of the gland and / or the lumen of the ducts. The 37 years old female patient, VBB, leucoderma, attended the stomatology service with a complaint of swelling in the floor of mouth, which she noticed 10 years ago. The clinical and radiographic exams indicated a diagnosis of multiple sialolithiasis in the left submandibular gland duct. Surgical intervention was indicated in this case. Amongst all sialolithiasis cases, 80% affect the submandibular glands. Of these, 70% are isolated sialoliths. Only 5% of cases present more than 3 calcifications. This study aims to report the diagnosis and treatment of a rare case of multiple sialoliths located in the duct of the submandibular gland, which were surgically removed via intraoral access.

Spontaneous Discharged Submandibular Gland Duct Sialolith: Α Rare Case Report

2019 ◽  
Vol 82 (2) ◽  
pp. 205-207
Author(s):  
Wentao Zhang ◽  
Kai Wang ◽  
Fan Yang
Keyword(s):  
Case Report ◽  
Submandibular Gland ◽  
Rare Case ◽  
Rare Case Report ◽  
Gland Duct

Intraglandular Tooth—Rare Case Report of Tooth in Submandibular Salivary Gland Duct

2011 ◽  
Vol 69 (9) ◽  
pp. e305-e307 ◽  
Author(s):  
D.S. Gupta ◽  
Padam N. Tandon ◽  
Shalender Sharma ◽  
Sunit K. Jurel ◽  
Kaberi Majumder
Keyword(s):  
Salivary Gland ◽  
Case Report ◽  
Rare Case ◽  
Submandibular Salivary Gland ◽  
Rare Case Report ◽  
Gland Duct

scholarly journals Spinal dysraphism with tripedus morphology: A case report

2021 ◽  
pp. 509-511
Author(s):  
Mohd Monis ◽  
Shagufta Wahab ◽  
Divyashree Koppal ◽  
Aiman Ibbrahim
Keyword(s):  
Case Report ◽  
Spina Bifida ◽  
Vertebral Column ◽  
Rare Case ◽  
Surgical Intervention ◽  
Spinal Dysraphism ◽  
Tethered Cord ◽  
Lower Back ◽  
Rare Case Report ◽  
Spinal Mri

This is a rare case report of a 5-month-old child with a complex spinal dysraphic state, and an accessory limb (tripedus morphology), accessory genitalia, and anal dimple. The child was brought to the hospital with an accessory limb arising from the back. On clinical examination, an accessory limb arising from the lower back with a partially developed foot with the presence of toes and nails was noted. Spinal MRI was advised which revealed dysraphic features including spina bifida with the low lying and posteriorly tethered cord with diastematomyelia along with a supernumerary appendage attached to the vertebral column having rudimentary bones resembling those of extremities. The presence of an accessory limb with spinal dysraphism is quite a rare anomaly. The condition can be treated by surgical intervention and involves excision of the accessory limb with adequate dural and paraspinal muscle cover.

scholarly journals Kuttner tumor involving minor salivary glands: A very rare case report

2014 ◽  
Vol 26 (1) ◽  
pp. 89
Author(s):  
Moni Thakur ◽  
VenkateswaraRao Guttikonda ◽  
Ramesh Thummala ◽  
VinayKumar Reddy Kundoor
Keyword(s):  
Case Report ◽  
Salivary Glands ◽  
Rare Case ◽  
Minor Salivary Glands ◽  
Rare Case Report ◽  
Küttner Tumor

scholarly journals Tuberculous Uveitis, Erythema Induratum, and Persistent Genital Warts in a Female Patient: A Rare Case Report

2019 ◽  
Vol 8 (1) ◽  
pp. 70
Author(s):  
Pedram Alirezaei ◽  
MohammadMahdi Majzoobi ◽  
Siamak Akbarzadeh ◽  
Golnoush Ebrahimi ◽  
HamidReza Ghasemibasir
Keyword(s):  
Case Report ◽  
Female Patient ◽  
Rare Case ◽  
Genital Warts ◽  
Tuberculous Uveitis ◽  
Rare Case Report

scholarly journals A rare case report of aplasia cutis congenita of the scalp with triplet skin defects in non-syndromic newborn

2021 ◽  
Vol 8 (3) ◽  
pp. 997
Author(s):  
Naim Sulaiman Abuzarifa ◽  
Wan Azman Wan Sulaiman
Keyword(s):  
Case Report ◽  
Gestational Age ◽  
Rare Case ◽  
Surgical Intervention ◽  
Skin Condition ◽  
Skin Defect ◽  
Aplasia Cutis Congenita ◽  
Skin Defects ◽  
Rare Case Report ◽  
Aplasia Cutis

Aplasia cutis congenita is an uncommon localized or widespread congenital skin condition characterized by the absence of the skin, and occasionally underlying tissues occurs in about one every 10.000 birth mostly in the scalp as single or more than one lesion and sometimes occurs in extremities and trunk with an uncertain cause and can be associated with numerous syndromes or can be sporadic which is diagnosed clinically and usually conservatively managed but sometimes surgical intervention needed. In this literature, we present nonsyndromic newborn Malay girl normally delivered with 35 weeks gestational age with triplet skin raw areas at the vertex of the scalp with well-demarcated defect round in shape measured about 0.5 in radius covered with a noninflammatory, necrotic patch. To our knowledge, many works of literatures presented Aplasia cutis congenita at the scalp with solitary single or occasionally more than one skin defect. In contrast, in our case, we present an infrequent rare case of triplet skin defect of aplasia cutis congenita for nonsyndromic newborns. 

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