scholarly journals Non Infiltrating Oral Angiolipoma – Report of A Rare Case with Review

2021 ◽  
Vol 14 (02) ◽  
pp. 1047-1050
Author(s):  
Sreeshyla HS ◽  
Priyanka Nitin ◽  
Usha Hegde ◽  
Vidya Gowdappa Doddawad ◽  
Premalatha Bidadi Rajashekaraiah
Keyword(s):  
Salivary Gland ◽  
Clinical Diagnosis ◽  
Buccal Mucosa ◽  
Rare Case ◽  
Clinical Presentation ◽  
Benign Tumors ◽  
Pathological Evaluation ◽  
Vascular Component ◽  
Conclusive Diagnosis

The clinical presentation of typical lipomas is often characteristic. But the variations of lipoma based on the associated stroma poses a challenging picture with clinical diagnosis varying from benign tumors, various inflammatory and reactive lesions, salivary gland lesions, to few peripheral odontogenic lesions. Only a thorough clinical and pathological evaluation and correlation will help in arriving at a conclusive diagnosis, in understanding the behaviour, planning the treatment and predicting the prognosis of the lesion. One such case of lipoma presenting as an unassuming swelling clinically, but showing exuberant vascular component occurring on buccal mucosa is presented. A review of this variant of lipoma is discussed in comparison with the present case.

scholarly journals Pleomorphic Adenoma of Minor Salivary Gland in Buccal Mucosa: an Uncommon Finding

2015 ◽  
Vol 03 (01) ◽  
pp. 047-050
Author(s):  
Gourav Ahuja ◽  
Jaideep Marya ◽  
Poonam Sood
Keyword(s):  
Salivary Gland ◽  
Salivary Glands ◽  
Pleomorphic Adenoma ◽  
Buccal Mucosa ◽  
Minor Salivary Gland ◽  
Salivary Gland Tumors ◽  
Benign Tumors ◽  
Minor Salivary Glands ◽  
Diverse Range ◽  
Neck Tumors

AbstractSalivary gland tumors account for less than 3% of the head and neck tumors. Among various salivary gland tumors, pleomorphic adenoma is most common and accounts for 60- 70% of the benign tumors of salivary glands. However, the involvement of minor salivary glands of buccal mucosa is extremely uncommon and reported to be 4% only. Salivary glands may present with a diverse range of lesions presenting a challenge to even the most experienced clinician. We report two rare cases of pleomorphic adenoma of minor salivary glands of buccal mucosa in a 45 year old female and 70 years old male respectively. It includes clinical features, diagnosis and treatment of the tumor.

scholarly journals A Rare Case Study of Torsion of a Non-Gravid Uterus

2018 ◽  
Vol 2 (3) ◽  
pp. 309-311
Author(s):  
Tulasa Basnet ◽  
Padam Raj Panta ◽  
Jyoti Sharma ◽  
Amrit Pokhrel
Keyword(s):  
Acute Abdomen ◽  
Clinical Diagnosis ◽  
Rare Case ◽  
Clinical Presentation ◽  
Abdominal Mass ◽  
Gravid Uterus ◽  
Ischemic Damage ◽  
Operative Finding ◽  
Uterine Torsion

Torsion of a non gravid uterus is a rare but potentially fatal event. It may lead to rapid clinical deterioration causing irreversible ischemic damage to the uterus. The rarity of the condition and its non specific clinical presentation make the clinical diagnosis difficult. In this report we discuss a case of uterine torsion in a 55 year old postmenopausal lady who presented in emergency with acute abdomen. On examination a huge abdominal mass arising from pelvis was noted. The operative finding was huge fundal myoma with uterine torsion.Birat Journal of Health SciencesVol.2/No.3/Issue 4/Sep- Dec 2017, Page: 309-311 

scholarly journals Isolated Plexiform Neurofibroma of the Tongue

2013 ◽  
Vol 5 (02) ◽  
pp. 127-129 ◽  
Author(s):  
Abhishek Sharma ◽  
Parama Sengupta ◽  
Anjan KR Das
Keyword(s):  
Malignant Transformation ◽  
Rare Case ◽  
Benign Tumor ◽  
Clinical Presentation ◽  
Plexiform Neurofibroma ◽  
Common Variant ◽  
Benign Tumors ◽  
Plexiform Neurofibromas ◽  
Neural Origin ◽  
Rare Benign Tumor

ABSTRACTNeurofibromas (NF) are benign tumors of neural origin, of which roughly 90% appear as solitary lesions. They are classified into cutaneous, subcutaneous, and plexiform subtypes. Plexiform neurofibromas are the least common variant and usually are pathognomonic for NF I. Here, we present a very rare case of isolated plexiform neurofibroma with a painless enlarging mass of the tongue of an 11-year-old girl. This rare benign tumor has the potential for malignant transformation, and the diagnosis was difficult owing to the patient's age and to the insidious clinical presentation. The present case is a diffuse isolated plexiform neurofibroma of the tongue that was not associated with neurofibromatosis that was treated with intraoral surgery.

scholarly journals Oral Mucocele of Unusual Size on the Buccal Mucosa: Clinical Presentation and Surgical Approach

2012 ◽  
Vol 6 (1) ◽  
pp. 67-68 ◽  
Author(s):  
Juliana Seo ◽  
Ingrid Bruno ◽  
Gabriela Artico ◽  
Aluana dal Vechio ◽  
Dante A Migliari
Keyword(s):  
Salivary Gland ◽  
Male Patient ◽  
Surgical Approach ◽  
Buccal Mucosa ◽  
Surgical Procedure ◽  
Clinical Presentation ◽  
Minor Salivary Gland ◽  
Complete Removal ◽  
Lower Lip ◽  
Preliminary Diagnosis

Oral mucoceles are small-size, benign minor salivary gland pathologies. The most frequent localizations of these lesions are the lower lip mucosa. However, in some cases, they grow to an unusual size and hinder the preliminary diagnosis of mucocele. The purpose of this article is to report a case of a large oral mucocele with a diameter of 3.5 cm on the buccal mucosa of a 43-years-old male patient. The surgical procedure was carried out for a complete removal of the lesion.

scholarly journals Evaluation of salivary gland tumors- clinically radiologically and pathologically: prospective study

2021 ◽  
Vol 7 (4) ◽  
pp. 575
Author(s):  
Namita Mishra ◽  
Neeta Sharma
Keyword(s):  
Salivary Gland ◽  
Diagnostic Accuracy ◽  
Clinical Presentation ◽  
Malignant Tumors ◽  
Needle Aspiration ◽  
Salivary Gland Tumors ◽  
Benign Tumors ◽  
Aspiration Cytology ◽  
Fine Needle ◽  
Needle Aspiration Cytology

<p><strong> </strong></p><p class="abstract"><strong>Background: </strong>Salivary gland tumors are difficult to differentiate based solely on clinical presentation or cytological findings due to their overlapping pictures. Often inadequate samples from cytology pose a challenge in preoperative diagnosis. Histopathology is considered the gold standard in diagnosing these tumors. The purpose of this study was to determine clinical, radiological, and cytological findings of these tumors and to assess the accuracy of these results with that of histopathological diagnosis.</p><p class="abstract"><strong>Methods: </strong>Prospectively 52 patients with salivary gland swellings were enrolled between 2007-2009. Cases with inflammatory swelling were excluded from the study. Demographic, clinical history, preoperatively ultrasonography, cytology, and histopathological data were collected and analyzed.</p><p class="abstract"><strong>Results: </strong>Most cases (65.38%) had parotid gland involvement. Benign tumors were common (80.76%) with pleomorphic adenoma as the most common one. Malignant tumors comprised 19.23%. Mucoepidermoid carcinoma and adenoid cystic carcinoma were common malignant tumors. Local swelling was the most common clinical presentation, and no facial nerve involvement was reported. The hard palate was the most common minor salivary gland affected predominantly by benign tumors. The diagnostic accuracy of fine-needle aspiration cytology was 96.15%, followed by clinical and radiological diagnostic accuracy of 92.31% and 86.54%, respectively. Using McNemar's test, a significant agreement was found between clinical and histological diagnosis (p=0.1336) and between FNAC and histological diagnosis (p=0.4975).</p><p class="abstract"><strong>Conclusions: </strong>Fine needle aspiration cytology is a highly accurate, sensitive, and specific screening technique. It is safe and reliable, though minimally invasive. Ultrasonography-guided cytology along with clinical, and radiological findings could enhance the pre-operative diagnostic accuracy in distinguishing salivary gland tumors.</p>

Monomorphic Adenoma of Posterior Palate: A Rare Case Report

2021 ◽  
Author(s):  
Abhinav Sharma
Keyword(s):  
Salivary Gland ◽  
Case Report ◽  
Rare Case ◽  
Malignant Tumors ◽  
Minor Salivary Gland ◽  
Benign Tumors ◽  
Rare Entity ◽  
Present Case Report ◽  
Rare Case Report ◽  
Monomorphic Adenoma

Background: Minor salivary gland benign tumors account for a very small percentage of salivary gland tumors of which monomorphic adenomas are a rare entity. Methods and Findings: The present case report discusses a rare case report of an 18-year-old female patient diagnosed with monomorphic adenoma of the posterior palatal region. The diagnosis was reached after thorough radiographical and pathological investigations. Conclusion: Monomorphic Adenoma in a younger individual is a rare disorder and can be used as a collective term for benign or malignant tumors comprising of one type or even two types of cells.

An Atypical Case of Renal Mass - A Case Study

2020 ◽  
Vol 15 (2) ◽  
pp. 56-58
Author(s):  
Shafiqur Rahman ◽  
B Ahmed ◽  
ATM Mowladad Chowdhury ◽  
Mirza M Hasan ◽  
Sayedul Islam
Keyword(s):  
Renal Cell Carcinoma ◽  
Cell Carcinoma ◽  
Clinical Diagnosis ◽  
Renal Cell ◽  
Renal Mass ◽  
Clinical Presentation ◽  
Atypical Case ◽  
Renal Tuberculosis

A forty eight year old woman with the clinical diagnosis of renal mass due to renal cell carcinoma was found to have renal tuberculosis. The clinical presentation and management are being discussed. Bangladesh Journal of Urology, Vol. 15, No. 2, July 2012 p.56-58

Large Vulvar Lipoma in an Adolescent: A Case Report

JMS SKIMS ◽  
2011 ◽  
Vol 14 (1) ◽  
pp. 28-29
Author(s):  
R K Maurya ◽  
Pawan Kumar Singh ◽  
Sandeep Singh
Keyword(s):  
Case Report ◽  
Epithelial Cell ◽  
Adolescent Girl ◽  
Rare Case ◽  
Mesenchymal Cell ◽  
Benign Tumors ◽  
Melanocytic Tumors

Lipomas of vulva have been reported only rarely. Benign tumors of the vulva are normally classified according to their origin as epithelial cell tumors (e.g., keratinocytic, adnexal and ectopic tumors), or mesenchymal cell tumors (e.g., vascular, fibrous, muscular, neural, adipose and melanocytic tumors). Vulvar lipomas need to be differentiated from liposarcomas, which are rare but are very similar to lipomas clinically. Here we present a rare case of large vulvar lipoma in an adolescent girl. JMS 2011;14(1):28-29

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