Mesenteric Artery Stenosis Presenting as Severe Erosive Gastroduodenitis: A Rare Case Report With Long Term Follow-Up

2015 ◽  
Vol 6 (4) ◽  
pp. 194-196
Author(s):  
Ramesh Dwarakaprasad ◽  
Huliyurdurga Srinivasa Setty Natraj Setty ◽  
Kumarswamy X ◽  
Sunil Kumar ◽  
Guruprasad X ◽  
...  
Keyword(s):  
Case Report ◽  
Mesenteric Artery ◽  
Rare Case ◽  
Artery Stenosis ◽  
Rare Case Report ◽  
Long Term Follow Up ◽  
Mesenteric Artery Stenosis

scholarly journals Granulocytic sarcoma in non-leukaemic child involving maxillary sinus with long term follow up: A rare case report

2014 ◽  
Vol 4 (1) ◽  
pp. 90 ◽  
Author(s):  
HarkanwalPreet Singh ◽  
AnishAshok Gupta ◽  
Parveen Garg ◽  
NinadJoshirao Moon ◽  
Rahul Chavan ◽  
...  
Keyword(s):  
Case Report ◽  
Maxillary Sinus ◽  
Rare Case ◽  
Granulocytic Sarcoma ◽  
Rare Case Report ◽  
Long Term Follow Up

scholarly journals Ossifying fibromyxoid tumor of the oral cavity: rare case report and long-term follow-up

2021 ◽  
Vol 11 ◽  
Author(s):  
Maria Eduarda Pérez-de-Oliveira ◽  
Thayná Melo de Lima Morais ◽  
Márcio Ajudarte Lopes ◽  
Oslei Paes de Almeida ◽  
Willie F. P. van Heerden ◽  
...  
Keyword(s):  
Case Report ◽  
Oral Cavity ◽  
Rare Case ◽  
Rare Case Report ◽  
Long Term Follow Up ◽  
Ossifying Fibromyxoid Tumor

scholarly journals Juvenile Aggressive Trabecular Ossifying Fibroma of Mandible: A Rare Case Report

2016 ◽  
Vol 6 (1) ◽  
pp. 45-51
Author(s):  
Deepa Das Achath ◽  
Abhishek Sanjay Ghule ◽  
Preeti Kanchan-Talreja ◽  
Sunanda Bhatnagar
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Histological Analysis ◽  
High Recurrence Rate ◽  
Ossifying Fibroma ◽  
Appropriate Treatment ◽  
Juvenile Ossifying Fibroma ◽  
Rare Case Report

ABSTRACT Fibroosseous lesions of the jaws, including juvenile ossifying fibroma (JOF), pose diagnostic and therapeutic difficulties due to their clinical, radiological, and histological variability. There are two histological varieties of it, one as psammomatoid type and second as trebacular type; here, we present a trebacular type, which is a rare variety. After the clinical examination, radiological and histological analysis, it was diagnosed as juvenile trebacular ossifying fibroma. Although JOF is an uncommon clinical entity, its aggressive local behavior and high recurrence rate means that it is important to make an early diagnosis, apply the appropriate treatment, and, especially, follow-up the patient over the long term. How to cite this article Ghule AS, Achath DD, Kanchan- Talreja P, Bhatnagar S. Juvenile Aggressive Trabecular Ossifying Fibroma of Mandible: A Rare Case Report. J Contemp Dent 2016;6(1):45-51.

scholarly journals Primary Tuberculous Lymphadenitis: a Rare Case Report

2018 ◽  
Vol 22 (2) ◽  
pp. 106-110
Author(s):  
Mustafa Mert Açikgöz ◽  
Ayşem Yurtseven ◽  
Gülsüm Ak
Keyword(s):  
Case Report ◽  
Multidisciplinary Approach ◽  
Maxillofacial Surgery ◽  
Excisional Biopsy ◽  
Oral And Maxillofacial Surgery ◽  
Tuberculous Lymphadenitis ◽  
Rare Case Report ◽  
Long Term Follow Up

SummaryBackground/Aim: Our aim is to describe multidisciplinary approach to primary tuberculous lymphadenitis with a case report.Case Report: A 6-year-old boy was referred to İstanbul University, Faculty of Dentistry, Department of Oral and Maxillofacial Surgery with the symptoms of painless extra-oral abscess and lymphadenopathy. The diagnosis of primary tuberculous lymphadenitis was proved by microbiological culture and ultrasound imaging.Conclusions: Combine tuberculosis treatment should be applied and long term follow up is necessary. Excisional biopsy for tissue diagnosis and bacterial examination with culture should be performed for an early diagnosis as a delay in treatment can lead to devastating consequences.

scholarly journals Transurethral resection of a bladder trigone leiomyoma: a rare case report

BMC Urology ◽  
2020 ◽  
Vol 20 (1) ◽  
Author(s):  
Athanasios Zachariou ◽  
Maria Filiponi ◽  
Fotios Dimitriadis ◽  
Aris Kaltsas ◽  
Nikolaos Sofikitis
Keyword(s):  
Case Report ◽  
Transurethral Resection ◽  
English Literature ◽  
Benign Tumors ◽  
Macroscopic Hematuria ◽  
Urinary Tract Symptoms ◽  
Rare Case Report ◽  
Long Term Follow Up

Abstract Background Bladder leiomyomas are rare and benign tumors of the bladder. They account for 0.43% of all bladder tumors, and only 250 cases have been reported in English literature. Based on the size and localization of the lesion, their symptoms vary considerably. Women seem to be more affected, and obstructive symptoms predominate. Surgical treatment is almost always highly effective, leaving a low recurrence rate. Case presentation We present a clinical case of a 52-year old man with macroscopic hematuria and obstructive lower urinary tract symptoms due to a large bladder trigone leiomyoma. CT and MRI showed a well-defined large bladder leiomyoma and cystoscopy established the initial findings. The patient underwent successful transurethral resection of the lesion, and pathology findings confirmed the diagnosis. Conclusions This case report demonstrates that transurethral resection of a large bladder trigone leiomyoma is a feasible and successful procedure. Long term follow-up proves that there is neither scarring distortion of the bladder trigone area nor damage in the ureteral orifices, even though there was a thorough removal of the trigone wall.

scholarly journals Thoracoscopic and laparoscopic resection of a huge oesophageal liposarcoma: a case report

2021 ◽  
Vol 49 (9) ◽  
pp. 030006052110412
Author(s):  
Rui Li ◽  
Chen Lin ◽  
Yuxun Huang ◽  
Liang Cao ◽  
Rui Hu ◽  
...  
Keyword(s):  
Case Report ◽  
Minimally Invasive ◽  
Rare Case ◽  
Laparoscopic Resection ◽  
Polypoid Mass ◽  
Current Case ◽  
Long Term Follow Up ◽  
History Of

Oesophageal liposarcomas are particularly rare, accounting for 1.2–1.5% of all gastrointestinal liposarcomas. Surgical resection is the usual treatment. Endoscopic resection is minimally invasive but still controversial. This current case report describes a rare case of a large oesophageal liposarcoma in a 52-year-old male that presented with 10-year history of dysphagia for dry and solid food that was exacerbated by a recent common cold. Thoracoscopic and laparoscopic oesophagectomy was performed. He did not have any dysphagia or dyspnoea 1 week postoperatively. The excised specimen consisted of a polypoid mass measuring 21.0 cm × 5.1 cm. Histological examination confirmed that it was an oesophageal liposarcoma. At 1-year postoperatively, there was no sign of recurrence. Thoracoscopy and laparoscopy can be used to treat large oesophageal masses. Long-term follow-up is required as oesophageal liposarcomas tend to recur.

scholarly journals Ameloblastic fibroma: A rare case report with 7-year follow-up

2015 ◽  
Vol 143 (3-4) ◽  
pp. 190-194 ◽  
Author(s):  
Araújo de ◽  
Adna Barros ◽  
Cássia de ◽  
Arlei Cerqueira ◽  
Dos Nunes
Keyword(s):  
Malignant Transformation ◽  
Rare Case ◽  
Case Reports ◽  
Permanent Teeth ◽  
Proliferation Index ◽  
Ameloblastic Fibroma ◽  
Rare Case Report ◽  
Long Term Follow Up

Introduction. Ameloblastic fibroma (AF) is a rare benign odontogenic tumor that usually occurs in the first two decades of life. It affects adolescents and young adults and is found in the mandible and with a higher frequency in the posterior region of this segment. There are rare case reports with a long-term follow-up. Case Outline. We report the case of a 6-year-old boy with extensive ameloblastic fibroma in the mandible. Treatment consisted of enucleation and bone curettage, with the preservation of permanent teeth adjacent to the tumor. Clinical and radiographic follow-up of the patient over a period of 7 years showed no signs of recurrence or malignant transformation. Conclusion. Patients with AF should be under follow-up for prolonged periods of time, even in cases exhibiting a low proliferation index, because of the potential for recurrence and malignant transformation of this tumor.

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