scholarly journals Tuberculous mastitis: a rare case report

2020 ◽  
Vol 9 (9) ◽  
pp. 3909
Author(s):  
Hind Ennasser ◽  
Jamal Eddine Raoudi ◽  
Hafsa Taheri ◽  
Hanane Saadi ◽  
Ahmed Mimouni
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Epithelioid Cell ◽  
Breast Abscess ◽  
Rare Entity ◽  
Granulomatous Mastitis ◽  
Clinical Issue ◽  
Rare Case Report ◽  
Radiological Aspect ◽  
Post Menopausal

Tuberculous mastitis is a granulomatous mastitis due to infection by mycobacterium tuberculosis. It’s a rare entity witch is often confused with breast carcinoma or pyogenic breast abscess because of its clinical and radiological aspect. The diagnosis is histological with identification of an epithelioid cell granulomas and necrosis. The treatment is based on anti-tuberculous therapy with a good clinical issue. Authors report a case of tubercular mastitis in a post-menopausal female diagnosed on adenectomy.

scholarly journals Dysgenetic Polycystic Disease of Minor Salivary Gland: A Rare Case Report and Review of the Literature

2017 ◽  
Vol 2017 ◽  
pp. 1-5
Author(s):  
N. Srikant ◽  
Shweta Yellapurkar ◽  
Karen Boaz ◽  
Mohan Baliga ◽  
Nidhi Manaktala ◽  
...  
Keyword(s):  
Differential Diagnosis ◽  
Salivary Gland ◽  
Case Report ◽  
Rare Case ◽  
Minor Salivary Gland ◽  
Rare Entity ◽  
Review Of The Literature ◽  
Lower Lip ◽  
Polycystic Disease ◽  
Rare Case Report

Polycystic (dysgenetic) disease of the salivary glands is a rare entity that has only recently been described in the literature. The disease is more commonly seen in females and majority of the cases have presented as bilateral parotid gland swellings. This case presenting in a 21-year-old male is the first of this unusual entity involving solely the minor salivary gland on the lower lip. This case report highlights the importance for the clinician to be aware of this differential diagnosis, when treating an innocuous lesion like a mucocele.

Intraoral Schwannoma: A Rare Case Report

2016 ◽  
Vol 1 (1) ◽  
pp. 20-22
Author(s):  
Ranjan Agrawal ◽  
Prashant Bhardwaj ◽  
Abhinav Srivastava
Keyword(s):  
Differential Diagnosis ◽  
Case Report ◽  
Rare Case ◽  
Rare Entity ◽  
Rare Occurrence ◽  
Floor Of The Mouth ◽  
Nerve Sheath ◽  
Rare Case Report ◽  
Sheath Cells

ABSTRACT Schwannomas or neurilemmomas are benign, encapsulated tumor arising from nerve sheath cells. Intracranial Schwannomas are most common with rare occurrence in the extracranial region. It rarely occurs in the floor of the mouth with very few cases reported. We present a rare case report of Schwannoma of the floor of the mouth, thereby highlighting the consideration of this rare entity as one of the differential diagnosis in cases who present to us with swelling of the floor of the mouth and also the importance of immunohistochemistry in coming to the diagnosis. How to cite this article Srivastava A, Mohan C, Bhardwaj P, Agrawal R. Intraoral Schwannoma: A Rare Case Report. Int J Adv Integ Med Sci 2016;1(1):20-22.

scholarly journals Dysembryoplastic neuropithelial tumor: a rare case report

2017 ◽  
Vol 5 (5) ◽  
pp. 2270
Author(s):  
Shailesh Thanvi ◽  
Hemant Jangid ◽  
Yogi Raj Joshi
Keyword(s):  
Young Adults ◽  
Case Report ◽  
Rare Case ◽  
Male Child ◽  
Adjuvant Chemoradiotherapy ◽  
Rare Entity ◽  
Intractable Seizures ◽  
Rare Case Report ◽  
Children And Young Adults ◽  
Space Occupying Lesion

Dysembryoplastic neuropithelial tumor (DNET) is a rare recently described, benign glioneural tumor frequently associated with intractable seizures in children and young adults which is important to recognise clinically and radiologically as it is surgically curable without need for adjuvant chemoradiotherapy. We hereby present a case report of a 10year old male child who presented with intractable seizures and right parietal space occupying lesion which was diagnosed DNET radiologically, treated by microsurgical excision and confirmed histopathologically as DNET, thus emphasising multidisciplinary role in management of this rare entity.

scholarly journals Perivascular Epithelioid Cell Tumor of the Kidney: A Rare Case Report

2017 ◽  
Vol 4 (3) ◽  
pp. 145-148
Author(s):  
Sedat Karakoç ◽  
Serdar Çelik ◽  
Ozan Bozkurt ◽  
Ömer Demir ◽  
Aykut Kefi ◽  
...  
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Epithelioid Cell ◽  
Cell Tumor ◽  
Perivascular Epithelioid Cell Tumor ◽  
Perivascular Epithelioid Cell ◽  
Rare Case Report

scholarly journals Isolated Sacrococcygeal Tuberculosis, A Case Report Of A Rare Atypical Presentation

2019 ◽  
Vol 1 (4) ◽  
Author(s):  
Daksh Gadi ◽  
Saket Nigam ◽  
Deepti Gupta ◽  
Akanksha Sinha
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Clinical Suspicion ◽  
Atypical Presentation ◽  
Rare Entity ◽  
Hematogenous Spread ◽  
Major Health Problem ◽  
Major Health ◽  
Rare Case Report ◽  
Atypical Presentations

Tuberculosis is a major health problem in India and in view of rise in the MDR tuberculosis atypical presentations are getting commoner these days and are difficult to diagnose. Musculoskeletal tuberculosis is very common among the  hematogenous spread cases of pulmonary tuberculosis involving thoracic spine the most. Involvement of sacrum and coccyx is rarest of  the possibility and isolated sacrococcygeal tuberculosis thus is very rare. Being a rare entity a high index of clinical suspicion is required to diagnose it. We hereby report a very rare case report of sacrococcygeal tuberculosis.

scholarly journals Placental Polyp : A Rare Case Report

2021 ◽  
Vol 20 (2) ◽  
pp. 85-88
Author(s):  
Most Sabina Yeasmin ◽  
Nishat Anjum Nourin ◽  
Tahera Begum ◽  
Farah Naz Mabud ◽  
Farjana Ahmed Surovi
Keyword(s):  
Case Report ◽  
Vaginal Bleeding ◽  
Rare Case ◽  
Histopathological Examination ◽  
Elevated Serum ◽  
Placental Tissue ◽  
Rare Entity ◽  
Definite Diagnosis ◽  
Rare Case Report ◽  
One Year

Placental polyp is the retained fragment of placental tissue which presents as a polypoidal or pedunculated mass within the uterus. It is a rare entity and has an incidence of less than 0.25 % of all pregnancies. There are also very few reported cases of the clinical placental polyp. Here,we report a case of 22-year-old P1 woman presenting with vaginal bleeding and something coming down into vagina.Her last pregnancy had occurred one year ago.Laboratory investigation revealed slightly elevated serum b-hCG. Ultrasonography revealed thick endometrium, broad cervix (5.2cm) and a hyperechoic mass within the cervix. Extraction of the placental polyp followed by endometrial curettage were done and tissue sent for histopathology. Definite diagnosis was made by histopathological examination and which was a placental polyp. Chatt Maa Shi Hosp Med Coll J; Vol.20 (2); July 2021; Page 85-88

scholarly journals High Grade Endometrial Stromal Sarcoma: a rare case report

2021 ◽  
Vol 16 (1) ◽  
Author(s):  
Snigdha Rai
Keyword(s):  
Prognostic Factors ◽  
Case Report ◽  
Surgical Management ◽  
Late Stage ◽  
Rare Case ◽  
Endometrial Stromal Sarcoma ◽  
High Grade ◽  
Rare Entity ◽  
Stromal Sarcoma ◽  
Rare Case Report

High grade endometrial stromal sarcoma (HG-ESS) is a very rare entity with poor outcome in compared to other endometrial stromal sarcoma as it is usually diagnosed in late stage. The stage of the disease, age and complete surgery are most important prognostic factors. Surgical management of a 40 years old lady with menometrorrhagia and high grade endometrial stromal sarcoma is presented.

scholarly journals Mixed Mucinous and Invasive Ductal Carcinoma of Male Breast: A Rare Case Report

2017 ◽  
pp. 1-4
Author(s):  
Kuldeep Ananda Vaidhya ◽  
Sukesh
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Ductal Carcinoma ◽  
Histopathological Examination ◽  
Mucinous Carcinoma ◽  
Male Breast ◽  
Rare Entity ◽  
Infiltrating Ductal Carcinoma ◽  
Rare Case Report ◽  
Desmoplastic Stroma

Male breast carcinoma is a rare entity. Here, we present a case of mixed mucinous carcinoma i.e. composite mucinous carcinoma with infiltrating ductal carcinoma component in a 55 year old man. Patient clinically presented with a lump in his right breast. Histopathological examination of the breast mass showed tumor cells arranged in nests, cords, cribriform pattern in a mucinous stroma and a part of tumor was showing features of infiltrating ductal carcinoma with desmoplastic stroma.

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