scholarly journals Multiple Intraoral Venous Malformations In A Geriatric Patient- A Rare Case Report

2018 ◽  
Vol 3 (1) ◽  
Keyword(s):  
Case Report ◽  
Venous Malformation ◽  
Dorsal Surface ◽  
Diagnostic Procedures ◽  
Ventral Surface ◽  
Clinical Findings ◽  
Clinical Aspects ◽  
Venous Malformations ◽  
Arteriovenous Anastomosis ◽  
Rare Case Report

Venous malformation (VM) is defined as a simple malformation with slow flow and an abnormal venous network. This is caused by a disturbance in the late stages of angiogenesis (trunal stage) resulting in the persistence of arteriovenous anastomosis present during embryonic life. This case report describes an unusual case of multiple intraoral venous malformations with questionable augmentation. A 65 year-old female had reported with a complaint of discomfort in mouth since 8 years. Intraoral examination revealed presence of six spherical swellings (three on dorsal surface of tongue, one on ventral surface of tongue and two on left buccal mucosa) with bluish-violet hue, approximately 2 to 3 cm in diameter each. On the basis of history and clinical findings, vascular malformation was provisionally suspected. Adequate imaging established the diagnosis. A review of clinical aspects, diagnostic procedures as well as therapeutic options currently available for venous malformations are discussed in this article.

scholarly journals Non-painful severe variant form of eruptive lingual papillitis: A case report and literature review

2021 ◽  
Vol 13 (2) ◽  
Author(s):  
Manal Ahmed Halwani
Keyword(s):  
Emergency Department ◽  
Case Report ◽  
Literature Review ◽  
Oral Hygiene ◽  
Rare Case ◽  
Dorsal Surface ◽  
Variant Form ◽  
Girl Child ◽  
Rare Case Report ◽  
History Of

Eruptive lingual papillitis is a common benign disorder manifested by inflammation of fungiform papillae on the dorsolateral surface of the tongue. Several variants of lingual papillitis have been reported since 1997, most or all of them with painful erythematous papules. Here we report a case of 6 years old girl child with non-painful severe variant form of eruptive lingual papillitis presented to the emergency department. The entire dorsal surface of the tongue was surfaced by 2-3mm by multiple erythematous papules and some with a white or yellowish colour. The papules were excessively inflamed, pigmented, aggregated, and crusted. The cause was idiopathic which resolved within ten days. The parent and patient were reassured with advice to practice oral hygiene. This is a rare case report describing non-painful lingual papillitis without a history of any prior episodes.

scholarly journals LIPOSARCOMA OF SPERMATIC CORD PRESENTING AS INDIRECT INGUINAL HERNIA- A RARE CASE REPORT

2011 ◽  
Vol 01 (01/03) ◽  
pp. 63-65
Author(s):  
Padma Shetty K. ◽  
Harish S. Permi ◽  
Michelle Mathias ◽  
Kishan Prasad ◽  
Teerthanath S. ◽  
...  
Keyword(s):  
Case Report ◽  
Inguinal Hernia ◽  
Spermatic Cord ◽  
Rare Case ◽  
Surgical Excision ◽  
Myxoid Liposarcoma ◽  
Clinical Findings ◽  
Inguinal Region ◽  
Indirect Inguinal Hernia ◽  
Rare Case Report

AbstractLiposarcoma in the inguinal region though rare are clinically significant lesions. Preoperative diagnosis is difficult since the clinical findings are very similar to that of inguinal hernia. We report a rare case of Liposarcoma of the spermatic cord in 85 year old male, clinically diagnosed as left sided indirect inguinal hernia. Surgical excision specimen showed multiple globular lipomatous masses which were yellowish and grey tan with areas of myxoid degeneration and necrosis seen. Microscopic examination showed adipocytes arranged in lobules with numerous blood vessels, lipoblasts and myxoid stroma confirming the diagnosis of myxoid liposarcoma. He is on regular follow up since two years without any recurrence or metastasis. Our case report highlights the importance of sampling and examination of fatty masses in the inguinal region to rule out the possibility of liposarcoma as they are mistaken for lipoma at surgery.

Intraoral Venous Malformation-A Case report

2021 ◽  
pp. 80-82
Author(s):  
B.V Subhash ◽  
Alba Dinesh ◽  
Seema Patil ◽  
Asha R Iyengar ◽  
Revan Kumar Joshi ◽  
...  
Keyword(s):  
Case Report ◽  
Oral Cavity ◽  
Vascular Malformations ◽  
Venous Malformation ◽  
Vascular Anomalies ◽  
Venous Malformations ◽  
Wide Spread ◽  
Facial Area ◽  
Ct And Mri

The vascular anomalies consist of vascular tumours and vascular malformations. One among these are the venous malformations which constitute about 40% of all vascular malformations. Usually, the venous malformations present as localized lesions in the form of swellings/nodules with phleboliths, are diagnosed by ultrasonography, CT and MRI. Summary: This is a report of a rare longstanding case of wide spread venous malformations of oral cavity and facial area with phleboliths.

scholarly journals Angina Bullosa Haemmorhagica on the Ventral Surface of the Tongue- a rare case report

2016 ◽  
Vol 4 (1) ◽  
Author(s):  
Karthik. R ◽  
Mohan N. ◽  
Ravikumar. P.T
Keyword(s):  
Case Report ◽  
Mucous Membrane ◽  
Rare Case ◽  
Ventral Surface ◽  
Oral Mucous Membrane ◽  
Rare Case Report

<div><p><em>Angina Bullosa Hemmorhagica is a condition affecting the oral mucous membrane characterised by the presence of oral subepithelial blood filled blisters that ruptures and heals spontaneously by itself without any scarring.</em></p></div>

scholarly journals Abdominal aortic aneurysm: Rupture of the anterior wall

2007 ◽  
Vol 60 (1-2) ◽  
pp. 80-84 ◽  
Author(s):  
Miroljub Draskovic ◽  
Sidor Misovic ◽  
Miodrag Jevtic ◽  
Momir Sarac
Keyword(s):  
Computed Tomography ◽  
Case Report ◽  
Imaging Techniques ◽  
Diagnostic Procedures ◽  
Anterior Wall ◽  
Aneurysm Rupture ◽  
Clinical Findings ◽  
Aortic Aneurysms ◽  
Diagnostic Tools ◽  
Abdominal Aortic

Introduction An aneurysm is a focal dilatation of an artery (aorta), involving an increase in diameter of at least 50% as compared to the expected normal diameter (over 3 cm). Abdominal aortic aneurysms (AAA) cause thousands of deaths every year, many of which can be prevented with timely diagnosis and treatment. AAA can be asymptomatic for many years, but in one third of patients whose aneurysm ruptured, the mortality rate is 90%. In the past, palpation of the abdomen was the preferred method for identifying AAA. However, diagnostic imaging techniques, such as ultrasonography and computed tomography are more accurate and offer opportunities for early detection of AAA. Case report This paper is a case report of an 83-year old female patient. She was admitted due to severe pain in the abdomen. We already knew about the AAA (from her medical history). After using all available diagnostic procedures, rupture or dissection of the AAA were not confirmed. The patient underwent emergency surgery. During the operation, rupture of the anterior wall of the aneurysm was found. The anterior wall was filled with parietal thrombus, which hermetically closed the perforation. The patient was successfully operated and recovered. Conclusion The aim of this case report was to point out that our diagnostic procedures failed to confirm the rupture of AAA. We decided to apply surgical treatment, based on medical experience, clinical findings, ultrasonography and computed tomography and during operation rupture of AAA was confirmed. Patients with an already diagnosed AAA, or patients with clinical picture of rupture or dissection, are in urgent need for surgery, no matter what diagnostic tools are being used.

scholarly journals Giant Perineal Solitary Fibrous Tumor: A Rare Case Report

2017 ◽  
Vol 2017 ◽  
pp. 1-6 ◽  
Author(s):  
Petronio Augusto de Souza Melo ◽  
Ana Maria Yoshino Bonifaci ◽  
Fabio da Silva Crochik ◽  
Claudio Bovolenta Murta ◽  
Joaquim Francisco de Almeida Claro ◽  
...  
Keyword(s):  
Case Report ◽  
Solitary Fibrous Tumor ◽  
Clinical Findings ◽  
Complete Resection ◽  
Anatomic Site ◽  
Contrast Enhanced Ct ◽  
Contrast Enhanced ◽  
Rare Case Report ◽  
Lymph Node Swelling ◽  
Fibrous Tumor

Background. Solitary fibrous tumor (SFT) is a fibroblastic mesenchymal tumor that was initially described from the pleura but currently arises at almost every anatomic site. It is usually benign, and surgical resection is curative. SFT involving the perineum is extremely rare. This is the third case report of a perineal SFT in the literature.Case Presentation. We reported an uncommon case of a 64-year-old man presenting with a huge perineal mass that started growing 3 years before his arrival in our service. He was asymptomatic. A contrast-enhanced CT scan revealed a heterogeneous well-circumscribed perineal mass with soft-tissue density. Invasion of the surrounding organs, distal metastasis, and lymph node swelling were absent. The complete resection of mass was done successfully. The specimen was a 23.0×14.0×8.0 cm encapsulated tumor. Mass weight was 1,170 g. After pathological analysis, we confirmed that the mass was a solitary fibrous tumor. The diagnosis was based on clinical findings and histological morphology and immunohistochemistry study.Conclusion. SFTs are usually indolent tumors with a favorable prognosis. The perineal location is extremely rare. Complete resection of the mass is the treatment of choice.

scholarly journals Primary intra osseous venous malformation of nasal bone: A rare case report

2014 ◽  
Vol 47 (03) ◽  
pp. 423-426 ◽  
Author(s):  
Ajit Kumar Pati ◽  
Bibhuti Bhusan Nayak ◽  
Arun Kumar Choudhury ◽  
Debesh Kumar Rout
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Venous Malformation ◽  
Nasal Bone ◽  
Port Wine Stain ◽  
Port Wine ◽  
Review Of Literature ◽  
Rare Phenomenon ◽  
Rare Case Report ◽  
Back Ground

ABSTRACTPrimary intra osseous venous malformation with involvement of nasal bone is a rare phenomenon. Nasal bone intraosseous venous malformation on a back ground of port wine stain of face has not been reported in the available literature. We report the very rare case of intraosseous venous malformation of left nasal bone developing on a background of port wine stain of face, its diagnosis, pathology, management and review of literature.

scholarly journals Low Flow Venous Malformation of the Buccal Mucosa Treated by Surgical Excision - A Rare Case Report

2017 ◽  
Vol 7 (1) ◽  
pp. 42-45
Author(s):  
Suresh V ◽  
Sathyanarayanan R ◽  
Deepika S ◽  
Venugopalan V
Keyword(s):  
Case Report ◽  
Buccal Mucosa ◽  
Rare Case ◽  
Venous Malformation ◽  
Surgical Excision ◽  
Low Flow ◽  
Rare Case Report
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