Right atrial fungal endocarditis with bilateral extensive pulmonary infiltration caused by Neoscytalidium dimidiatum in an immunocompetent child: first case report from India

2015 ◽  
Vol 32 (1) ◽  
pp. 23-26 ◽  
Author(s):  
Ramesh Chandra Mishra ◽  
Ramachandra Barik ◽  
Mohd Abiduddin Arif ◽  
Amaresh Rao Malempati
Author(s):  
Pallavi Punhani ◽  
Neha Madan ◽  
Satnam Kaur ◽  
Sunil Ranga

Toxoplasmosis is a parasitic infection caused by the protozoan, Toxoplasma gondii which is an obligate intracellular parasite. Among all the parasites known to cause myocarditis or pericarditis, the most commonly found is Chaga’s Disease or American Trypanosomiasis. Several other parasites including T. gondii can affect the heart in immunocompromised patients. Individuals with intact immunity largely remain asymptomatic. Only 22 cases of Toxoplasma Pericarditis have been reported worldwide. Although, CNS and Ocular Toxoplasmosis cases have been reported from Indian subcontinent, there is a lack of literature on cardiac involvement by Toxoplasma. Here, we present a case of a   11 yr old immunocompetent child with Toxoplasma Pericarditis, the first case to be reported from India. An echocardiography confirmed diagnosis of pericardial effusion for which pericardiocentesis was done and sent to our department for cytological evaluation. Fluid was exudative with pericardial fluid to serum protein ratio of 0.7. Gram stain, AFB stain and CB NAAT of pericardial fluid were negative. Cytology revealed neutrophils and macrophages showing presence of intracellular organisms resembling tachyzoites of Toxoplasma species on the Giemsa stained smear. These tachyzoites were crescent shaped with one pointed end and the other rounded end and a central nuclei. A final diagnosis of Toxoplasma Pericarditis was made based on microscopy findings.  T. gondii serological tests were also done which showed positivity for IgG with strong avidity. Thus, our case report represents an important differential that should be considered by all the clinicians in cases of acute pericarditis, especially in difficult cases where no other cause can be identified.


2009 ◽  
Vol 19 (2) ◽  
pp. 138-142 ◽  
Author(s):  
Z.U. Khan ◽  
S. Ahmad ◽  
L. Joseph ◽  
R. Chandy

Author(s):  
Rahman Maraqa Sima Abdel ◽  
Robert McMahon ◽  
Anusha Pinjala ◽  
Gastelum Alheli Arce ◽  
Mohsen Zena
Keyword(s):  

2004 ◽  
Vol 7 (4) ◽  
pp. E312-E314 ◽  
Author(s):  
Ugur Filizcan ◽  
Sebnem Cetemen ◽  
Yavuz Enç ◽  
Mahmut Çakmak ◽  
Onur Göksel ◽  
...  

Author(s):  
Alaa AlAyed ◽  
Manar Samman ◽  
Abdul Peer-Zada ◽  
Mohammed Almannai
Keyword(s):  

Background: Binasal Occlusion (BNO) is a clinical technique used by many neurorehabilitative optometrists in patients with mild traumatic brain injury (mTBI) and increased visual motion sensitivity (VMS) or visual vertigo. BNO is a technique in which partial occluders are added to the spectacle lenses to suppress the abnormal peripheral visual motion information. This technique helps in reducing VMS symptoms (i.e., nausea, dizziness, balance difficulty, visual confusion). Case Report: A 44-year-old AA female presented for a routine eye exam with a history of mTBI approximately 33 years ago. She was suffering from severe dizziness for the last two years that was adversely impacting her ADLs. The dizziness occurred in all body positions and all environments throughout the day. She was diagnosed with vestibular hypofunction and had undergone vestibular therapy but reported little improvement. Neurological exam revealed dizziness with both OKN drum and hand movement, especially in the left visual field. BNO technique resulted in immediate relief of her dizziness symptoms. Conclusion: To our knowledge, this is the first case that illustrates how the BNO technique in isolation can be beneficial for patients with mTBI and vestibular hypofunction. It demonstrates the success that BNO has in filtering abnormal peripheral visual motion in these patients.


2020 ◽  
Vol 24 (1) ◽  
pp. 105-107
Author(s):  
Sedighe Shahhosseini ◽  
Reza Aminnejad ◽  
Amir Shafa ◽  
Mehrdad Memarzade

Carvajal syndrome is a rare genetic disorder. Patients reporting for surgery pose some difficulties in anesthesia management. In this case report we present the case of a 12-year-old boy, who was a known case of Carvajal syndrome, referred for surgical resection of perianal condyloma. Close monitoring of hemodynamic status is the mainstay of anesthetic considerations in such patients. As in any other challenging scenario, it should be kept in mind that ‘there is no safest anesthetic agent, nor the safest anesthetic technique; there is only the safest anesthesiologist’. Citation: Shahhosseini S, Aminnejad R, Shafa A, Memarzadeh M. Anesthesia in Carvajal syndrome; the first case report. Anaesth pain intensive care 2020;24(1):___ DOI: https://doi.org/10.35975/apic.v24i1.


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