A Rare Case Report of Anterior Chest wall Cold Abscess at Alluri Sita Rama Raju Academy of Medical Sciences, Eluru

2014 ◽  
Vol 2 (1) ◽  
pp. 61
Author(s):  
J R K Lande ◽  
K Chandra Sekhar ◽  
Narendra Valluri ◽  
Siva Rama Prasad Komera ◽  
P G Deotale
2014 ◽  
Vol 3 (4) ◽  
pp. 332
Author(s):  
Shivani Sood ◽  
Neelam Gupta ◽  
Sudarshan Sharma ◽  
Kavita Mardi

2014 ◽  
Vol 6 (3) ◽  
pp. 84-86
Author(s):  
Sonam Sharma ◽  
Amita Sharma ◽  
Ashok Kumar ◽  
Shivani Kalhan ◽  
Jasmine Kaur

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


2015 ◽  
Vol 33 (9) ◽  
pp. 1328.e3-1328.e5 ◽  
Author(s):  
Po-Chin Yu ◽  
Tzu-Hsien Yang ◽  
Abhishek Katakwar ◽  
Yu-Jen Cheng ◽  
Po-Chih Chang

Author(s):  
Maimoona Saeed ◽  
Iqtada Haider Shirazi

Abstract We report the case of a 12 days old baby boy who presented with swelling and bluish discoloration on his left hip at Pakistan Institute of Medical Sciences in November 2018. Ultrasound (USS) was useful in making the diagnosis of a neonatal psoas abscess. He was treated with extraperitoneal drainage and with systemic antibiotics. The clinical presentation and diagnosis, treatment of this rare condition and brief literature review is given in this case report. Key Words: Abscess, Iliopsoas, Neonate, Staphylococcus aureus, Extraperitoneal Drainage. Continuous....


2015 ◽  
Vol 2 (5) ◽  
pp. 597-601 ◽  
Author(s):  
Waddi Sudhakar ◽  
Venkata Rao B ◽  
Abburi Srinivas ◽  
Harshavarsan Majety S R ◽  
Madhulika M

2014 ◽  
Vol 2 (1) ◽  
pp. 35-37
Author(s):  
G Dewan

Association of hypercalcemia with SLE is very rare. Since initial report in 1991 only hand full cases have been described mainly in adult patients sporadically. Three pattern observed in this rare presentation. Commonly it is associated with serositis and lymphadenopathy or lymphedema known as hypercalcemia-lymphadenopathy SLE {HL-SLE) or hypercalcemia- lymphedema syndrome. Second group do not show this particular association. Concomitant primary hyperparathyroidism is responsible for third variety. This report describes a case of hypercalcemia associated with SLE from Bangladesh. DOI: http://dx.doi.org/10.3126/jucms.v2i1.10490   Journal of Universal College of Medical Sciences (2014) Vol.2(1): 35-37


Author(s):  
Anika Mittal ◽  
Ramesh Kumar Kundal ◽  
Harpal Singh Seemar ◽  
Puneet Garg ◽  
Namarta Goyal ◽  
...  

2017 ◽  
Vol 4 (10) ◽  
pp. 3526 ◽  
Author(s):  
Reshma S. ◽  
Vijai R. ◽  
Chakarvarthy N.

Poland’s syndrome is a rare congenital condition. It is classically characterized by absence of unilateral chest wall muscles and sometimes ipsilateral symbrachydactyly (abnormally short and webbed fingers). The condition typically presents with unilateral absence of the sternal or breast bone portion of the pectoralis major muscle which may or may not be associated with the absence of nearby musculoskeletal structures. We report a 25-year-old male patient with typical features of Poland’s syndrome. To the best of our knowledge, this is the first documented case of a patient with Poland’s syndrome reported from Chennai.


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