scholarly journals A RARE CASE OF INFECTIVE ENDOCARDITIS FOLLOWING CORONARY ANGIOPLASTY WITH AN UNUSUAL PRESENTATION OF ENDOPHTHALMITIS

2021 ◽  
Vol 39 (Supplement 1) ◽  
pp. e199
Author(s):  
Monisha D'souza ◽  
Roshan M
2020 ◽  
Vol 15 (3) ◽  
pp. 222-226 ◽  
Author(s):  
Asha K. Rajan ◽  
Ananth Kashyap ◽  
Manik Chhabra ◽  
Muhammed Rashid

Rationale: Linezolid (LNZ) induced Cutaneous Adverse Drug Reactions (CADRs) have rare atypical presentation. Till date, there are very few published case reports on LNZ induced CADRs among the multidrug-resistant patients suffering from Infective Endocarditis (MDR IE). Here, we present a rare case report of LNZ induced CARs in a MDR IE patient. Case report: A 24-year-old female patient was admitted to the hospital with chief complaints of fever (101°C) associated with rigors, chills, and shortness of breath (grade IV) for the past 4 days. She was diagnosed with MDR IE, having a prior history of rheumatic heart disease. She was prescribed LNZ 600mg IV BD for MDR IE, against Staphylococcus coagulase-negative. The patient experienced flares of cutaneous reactions with multiple hyper-pigmented maculopapular lesions all over the body after one week of LNZ therapy. Upon causality assessment, she was found to be suffering from LNZ induced CADRs. LNZ dose was tapered gradually and discontinued. The patient was prescribed corticosteroids along with other supportive care. Her reactions completely subsided and infection got controlled following 1 month of therapy. Conclusion: Healthcare professionals should be vigilant for rare CADRs, while monitoring the patients on LNZ therapy especially in MDR patients as they are exposed to multiple drugs. Moreover, strengthened spontaneous reporting is required for better quantification.


Author(s):  
Mohanambal M. ◽  
Wills G. Sheelaa

Mullerian anomalies occur in 1:1000-3000 females. Uterus didelphys and obstructed hemangioma with a septum contribute to 10% anomalies. Young girls present with severe dysmenorrhea, hematometra, hematocolpos and recurrent pregnancy loss. A 16-year-old teenager presented like a torsion of complex ovarian tumour is presented here. Intra operative findings was uterus didelphys with well-developed 2 horns, tubes and ovaries. On left ovary, a hemorrhagic corpus luteal cyst of size 5.2*4cm was seen with 50ml of hemoperitoneum. Diagnosis was confirmed histopathologically. This case is reported for the unusual presentation of an anomalous uterus mimicking torsion ovarian tumour.


2015 ◽  
Vol 7 (4) ◽  
pp. 520 ◽  
Author(s):  
ShyamM Talreja ◽  
Indraneel Banerjee ◽  
SherSingh Yadav ◽  
Vinay Tomar

2013 ◽  
Vol 345 (6) ◽  
pp. 507-508 ◽  
Author(s):  
Sameer Chadha ◽  
On Chen ◽  
Vijay Shetty ◽  
Adnan Sadiq ◽  
Gerald Hollander ◽  
...  

2016 ◽  
Vol 6 (3) ◽  
pp. 186 ◽  
Author(s):  
Suleiman Lawal ◽  
PhilipO Ibinaiye ◽  
AhmadT Lawal ◽  
MuhammadI Zaria ◽  
JosephB Igashi

2020 ◽  
Vol 2020 ◽  
pp. 1-2
Author(s):  
Fatemeh Mohaghegh ◽  
Akramsadat Amiri ◽  
Farahnaz Fatemi Naeini ◽  
Parvin Rajabi ◽  
Maryam Soltan

Eruptive syringoma is a rare variant of syringoma presenting with skin-colored or slightly pigmented papules mostly before or during puberty. In this report, we presented a rare case of eruptive syringoma in a 30-year-old woman. She exhibited multiple skin lesions in dorsal areas of her both hands, developed from the age of 15.


CHEST Journal ◽  
2018 ◽  
Vol 154 (4) ◽  
pp. 253A
Author(s):  
KIMBERLEY COUSINS ◽  
FUNMILOLA OGUNDIPE ◽  
NITHEESHA GANTA ◽  
WAYNE DAVIS

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