scholarly journals Sacrococcygeal Teratoma in Adult Female: A Case Report and Review of Literature.

2013 ◽  
Vol 12 (5) ◽  
pp. 31-34
Author(s):  
Tabowei B.I ◽  
2011 ◽  
Vol 1 (5) ◽  
pp. 164-165
Author(s):  
Dr. Yavalkar PA Dr. Yavalkar PA ◽  
◽  
Dr. Naik AM Dr. Naik AM

2019 ◽  
Vol 10 (03) ◽  
pp. 197-202
Author(s):  
Yasutake Uchima ◽  
Naoki Aomatsu ◽  
Takuma Okada ◽  
Hironari Miyamoto ◽  
Gen Tsujio ◽  
...  

2019 ◽  
Vol 54 ◽  
pp. 47-50 ◽  
Author(s):  
Nawaf Jaber Shatnawi ◽  
Muhammad Rushdi Khammash ◽  
Abdelkarim Hussein Omari

2019 ◽  
Vol 40 (4) ◽  
pp. 573
Author(s):  
RajkumarMotiram Meshram ◽  
R Nikila ◽  
Nilesh Nagdive

2014 ◽  
Vol 2 (10) ◽  
pp. 476-479
Author(s):  
Sandesh V. Parelkar ◽  
Beejal V. Sanghvi ◽  
Neha Sisodiya ◽  
Shalil H. Patil ◽  
Satej S. Mhaskar ◽  
...  

2021 ◽  
Vol 8 (5) ◽  
pp. 1646
Author(s):  
Suhail M. Khan ◽  
Azhar A. Khan ◽  
Anzeen N. Kanth ◽  
Aymen M. Khan ◽  
Irfita N. Kanth

Sacrococcygeal teratoma (SCT) is derived from embryonic germ cell layers and is one of the commonest tumours in infants. It is the most commonly occurring solid congenital tumours in the foetus and the new born. It is very rare in adults with less than a hundred cases documented in literature, with even rarer cases of male presentation. We report a case of a 26-year-old adult male presenting with a sacrococcygeal teratoma who was treated in our hospital along with its literature review.


2018 ◽  
Vol 7 (4) ◽  
pp. 47
Author(s):  
Shailesh Solanki

Sacrococcygeal teratoma (SCT) is the most common tumor of the newborn. Diagnosis is clinical and frequently straightforward. However, varied presentations can occasionally result in a diagnostic dilemma. We present a case of ruptured cystic Altman Type 1 SCT along with pertinent review of literature. The purely cystic variant of SCT is rare in itself and presenting as a ruptured lesion added to the dilemma in diagnosis and management.


2015 ◽  
Vol 6 (3) ◽  
pp. 125-127
Author(s):  
Sunita Chhapola ◽  
Inita Matta

ABSTRACT Introduction We report a rare case of isolated parotid abscess due to Mycobacterium fortuitum in an immunocompetent adult female, which to the best of our knowledge (on internet search) is the first case of its type. Methodology Diagnosis was based on MTBDR CM assay (Hain's) culture, followed by a positive TBAg MPT64 culture for MOTT. The patient was treated with abscess drainage and antibiotics with good results. A parotidectomy was not required in our patient. Conclusion Mycobacterium fortuitum parotid abscess is very rare. A knowledge of the pathogenicity of this organism and careful culture methods seem to be the key of accurate diagnosis. Treatment protocols are still subject to research. How to cite this article Chhapola Shukla S, Matta I. Mycobacterium Fortuitum causing Isolated Parotid Abscess in an Immunocompetent Adult Female: A Case Report and Review of Literature. Int J Head Neck Surg 2015;6(3):125-127.


2020 ◽  
Vol 4 (2) ◽  
pp. 286-288
Author(s):  
Ankit Lalchandani ◽  
Anjaly Mohan ◽  
Pradeep Saxena

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