scholarly journals Cutaneous sarcoidosis with protean manifestations: a rare case report

2019 ◽  
Vol 5 (2) ◽  
pp. 437
Author(s):  
Avinash Pravin ◽  
Shreya Srinivasan ◽  
Jayakar Thomas
Keyword(s):  
Case Report ◽  
Male Patient ◽  
Rare Case ◽  
Unknown Origin ◽  
Granulomatous Disease ◽  
Skin Involvement ◽  
Cutaneous Sarcoidosis ◽  
Rare Case Report ◽  
Systemic Manifestations ◽  
Systemic Sarcoidosis

<p class="abstract">Sarcoidosis is a multisystem granulomatous disease of unknown origin. The lung is the most commonly affected organ, but skin is frequently involved. Skin involvement is important because it may be the presenting sign of systemic sarcoidosis. Here, we report a rare case of sarcoidosis with systemic manifestations, in a 39 year old male patient.</p>

scholarly journals Pyogenic granuloma of tongue: A rare case report

2014 ◽  
Vol 6 (3) ◽  
pp. 84-86
Author(s):  
Sonam Sharma ◽  
Amita Sharma ◽  
Ashok Kumar ◽  
Shivani Kalhan ◽  
Jasmine Kaur
Keyword(s):  
Differential Diagnosis ◽  
Case Report ◽  
Male Patient ◽  
Rare Case ◽  
Pyogenic Granuloma ◽  
Definitive Diagnosis ◽  
Medical Sciences ◽  
New Approaches ◽  
Rare Case Report ◽  
Chronic Irritation

Pyogenic granuloma (PG) is a kind of inflammatory hyperplasia in response to chronic irritation. Here, we report a case of 64 year old male patient with PG on midline of the dorsum of the posterior third of the tongue. Its differential diagnosis, the importance of biopsy findings in establishing definitive diagnosis and about the new approaches for its treatment is discussed. DOI: http://dx.doi.org/10.3126/ajms.v6i3.10619Asian Journal of Medical Sciences Vol.6(3) 2015 84-86

scholarly journals AGGRESSIVE MESENTRIC FIBROMATOSIS: A RARE CASE REPORT AND REVIEW OF LITERATURE

2013 ◽  
Vol 03 (01) ◽  
pp. 79-82
Author(s):  
Rohan Shetty ◽  
Shubha Bhat ◽  
Rajesh Ballal ◽  
Pramod Makannavar ◽  
Anil Kumar K. N.
Keyword(s):  
Case Report ◽  
Male Patient ◽  
Rare Case ◽  
Clinical Presentation ◽  
Aggressive Fibromatosis ◽  
Definitive Diagnosis ◽  
Review Of Literature ◽  
Therapeutic Challenge ◽  
Rare Case Report ◽  
Small Intestinal

AbstractMesentric fibromatosis is a proliferative fibroblastic neoplasm of the small intestinal mesentery with varied clinical presentation. Giant mesentric fibromatosis is uncommon and its rarity poses a diagnostic and therapeutic challenge. This paper presents a recurrent aggressive fibromatosis in a 38 year old male patient, who had initially undergone a laparotomy outside for mass abdomen but only pus was evacuated and definitive diagnosis was not made.

scholarly journals Congenital Microphthalmia with Intraorbital Cyst: A Rare Case Report

2019 ◽  
Vol 2019 ◽  
pp. 1-3
Author(s):  
Bishow Raj Timalsina ◽  
Gulshan Bahadur Shrestha ◽  
Madhu Thapa
Keyword(s):  
Case Report ◽  
Congenital Malformation ◽  
Male Patient ◽  
Rare Case ◽  
Congenital Cataract ◽  
Orbital Tumor ◽  
Rare Case Report

Microphthalmia is considered to be the most common congenital malformation of the eye after congenital cataract. However, its association with intraorbital cyst is considered to be very rare. Most of the lesions are still misdiagnosed as orbital tumor and teratomas as there is a general paucity of data reported in literature. Herein, we report a rare case of congenital microphthalmia with intraorbital cyst in an eight-month-old male patient.

scholarly journals ILEOCOLIC INTUSSUSCEPTION: A RARE CASE REPORT OF MULTI-SYSTEMIC SARCOIDOSIS

CHEST Journal ◽  
2020 ◽  
Vol 158 (4) ◽  
pp. A1997
Author(s):  
Yuri Choi ◽  
Nazir Lone ◽  
Nancy Bethuel
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Ileocolic Intussusception ◽  
Rare Case Report ◽  
Systemic Sarcoidosis

scholarly journals Lipoma in Penis : A Rare Case Report

2013 ◽  
Vol 3 (1) ◽  
pp. 24-25
Author(s):  
T Ahmed ◽  
MA Kalam ◽  
II Mannan ◽  
MA Simi
Keyword(s):  
Case Report ◽  
Plastic Surgery ◽  
Male Patient ◽  
Rare Case ◽  
Young Male ◽  
Histopathological Analysis ◽  
Review Of The Literature ◽  
Ventral Aspect ◽  
Rare Case Report ◽  
Pedunculated Tumor

In this article we report one case of lipoma of the penis in a twenty three years old young male. This site of lipoma is rare. A case of a young male patient who consulted for removal of a penile lump is presented. The small, regular, wellcircumscribed pedunculated tumor localized on the ventral aspect of the penis was excised. The histopathological analysis showed a benign lipoma. A review of the literature showed lipoma of the penis to be very uncommon. For this reason, we were prompted to report this case.DOI: http://dx.doi.org/10.3329/bdjps.v3i1.15003 Bangladesh Journal of Plastic Surgery 2012, 3(1): 24-25

Hepatic adenoma in an elderly male patient: A rare case report

2014 ◽  
Vol 3 (2) ◽  
pp. 488
Author(s):  
Ravi Swami ◽  
RC Nimbargi ◽  
MN Karandikar ◽  
KA Jagdale
Keyword(s):  
Case Report ◽  
Male Patient ◽  
Rare Case ◽  
Hepatic Adenoma ◽  
Elderly Male ◽  
Rare Case Report
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