Extensive morphea profunda with autoantibodies and benign tumors: A rare case report

Primary pulmonary meningiomas are rare and mostly benign tumors. They usually appear as a solid peripheral pulmonary nodule on chest radiography and computed tomography and are frequently diagnosed incidentally. Herein, we report a 55-year-old female case of primary pulmonary meningioma mimicking pulmonary metastasis.

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Monomorphic Adenoma of Posterior Palate: A Rare Case Report

Journal of Dentistry and Oral Sciences ◽

10.37191/mapsci-2582-3736-3(2)-082 ◽

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.

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Peripheral Giant Cell Reparative Granuloma of the Sino-orbital Region—A Giant Lesion: A Rare Case Report

Otorhinolaryngology Clinics - An International Journal ◽

10.5005/jp-journals-10003-1169 ◽

2014 ◽

Vol 6 (3) ◽

pp. 109-113

Author(s):

Gaurav Ashish ◽

Anne Jenifer Prabhu ◽

Sunithi Mani

Keyword(s):

Case Report ◽

Giant Cell ◽

Rare Case ◽

Lateral Displacement ◽

Benign Tumors ◽

Giant Cell Reparative Granuloma ◽

Recurrence Rates ◽

Orbital Mass ◽

Rare Case Report ◽

Orbital Region

ABSTRACT Peripheral giant cell reparative granulomas (PGCRGs) are benign tumors which spread locally and progress aggressively. The origin of the multinucleated giant cells is not established till date, and hence various theories suggesting the origin from osteoclasts based on the immunohistochemical features, or from mononuclear phagocyte system. The treatment of choice is surgical excision with adequate margins and the recurrence rates are usually below 10% as per the reported literature.1 We present a 6-year-old child who presented with a rapidly progressive sino-orbital mass leading to proptosis and lateral displacement of the right globe. He underwent combined approach (open and endoscopic assisted) for complete excision of the lesion. The histopathological features were consistent with PGCRG. This case is being highlighted with the aim of developing insights about the clinical presentation and management of PGCRG. How to cite this article John M, Ashish G, Prabhu AJ, Mani S, Kurien M. Peripheral Giant Cell Reparative Granuloma of the Sino-orbital Region—A Giant Lesion: A Rare Case Report. Int J Otorhinolaryngol Clin 2014;6(3):109-113.

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Triplicity—Threefold of Skull Base Tumor—Atypic Meningioma Sphenoidal Wing Left, Low-Grade Olfactory Neuroblastoma of Sphenoidal Sinuses, Neurinoma N VIII. SIN. Very Rare Case Report

10.1055/s-0040-1702688 ◽

2020 ◽

Author(s):

Jan Hemza

Keyword(s):

Case Report ◽

Skull Base ◽

Rare Case ◽

Olfactory Neuroblastoma ◽

Low Grade ◽

Skull Base Tumor ◽

Rare Case Report

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Large Vulvar Lipoma in an Adolescent: A Case Report

JMS SKIMS ◽

10.33883/jms.v14i1.69 ◽

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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