scholarly journals Rare case of pulmonary histoplasmosis complicated with bronchocentric granulomatosis in a non endemic area

2017 ◽  
Vol 22 ◽  
pp. 1-3 ◽  
Author(s):  
Evanthia Botsa ◽  
Ioanna Thanou ◽  
Stamatina Kabanarou ◽  
Loukas Thanos
2017 ◽  
Vol 7 (3) ◽  
pp. e45-e45
Author(s):  
Ayyappan Vijayachandran Nair ◽  
Vidya Menon ◽  
Chandrababu K. Kumaran ◽  
Prince Shanavas Khan ◽  
Bhaskaran V. Kochukunju ◽  
...  

CHEST Journal ◽  
2020 ◽  
Vol 158 (4) ◽  
pp. A451
Author(s):  
Ahmad Raza ◽  
Adrian Estepa ◽  
Vincent Chan

2017 ◽  
Vol 11 (7) ◽  
pp. e0005558 ◽  
Author(s):  
Sri Krishna ◽  
Sneha Bhandari ◽  
Praveen K. Bharti ◽  
Sanjay Basak ◽  
Neeru Singh

2019 ◽  
Vol 25 (2) ◽  
pp. 150-152
Author(s):  
Mustafa Kuzucuoglu ◽  
◽  
Yesim Alpay ◽  
Figen Aslan ◽  
Derya Aydin ◽  
...  

Author(s):  
Misagh Shafizad ◽  
Saeid Ehteshami ◽  
Hamidreza Shojaei ◽  
Reza Jalili Khoshnoud

We report a rare case of cervical epidural abscess at the C5-C6 levels. The patient underwent surgery with complete abscess removal through C6 vertebral body corpectomy. The result of bacteriological culture was Brucella melitensis. Brucellosis must be considered as a possible cause of epidural abscess in patients from endemic area.


2008 ◽  
Vol 44 (10) ◽  
pp. 567-570 ◽  
Author(s):  
Manuel García-Marrón ◽  
José María García-García ◽  
Mercedes Pajín-Collada ◽  
Fernando Álvarez-Navascués ◽  
Manuel A. Martínez-Muñiz ◽  
...  

2019 ◽  
Vol 9 (3) ◽  
Author(s):  
Ritesh Neupane ◽  
Munish Sharma ◽  
Divakar Sharma ◽  
Rajeev Thachil ◽  
Mahesh Krishnamurthy ◽  
...  

Primary pulmonary histoplasmosis is found worldwide, and is particularly endemic in some areas of the North America, usually those surrounding the Ohio and Mississippi river valleys. It is not common in the East Coast of the United States, and is in fact, reportable in Pennsylvania. It has been rarely described in immunocompetent individuals residing in a non-endemic region. We present a case of a previously healthy middle-aged male, a Pennsylvania resident, who presented with mid-sternal chest discomfort, fatigue, chills and mild shortness of breath, and was diagnosed with primary pulmonary histoplasmosis.


2021 ◽  
pp. 1-3
Author(s):  
Maram Z. Nached ◽  
Labib S. Al-Ozaibi

Lymphatic filariasis is a common tropical parasitic infection caused by the Nematoda Filarioidae family. Filariasis predominantly affects the lymphoreticular system, leading to lymphedema, elephantiasis, hydrocele, and chyluria. However, its presentation as retroperitoneal cyst is very rare with a reported incidence rate of 1/105,000. We present a rare case of a previously healthy 26-year-old male presenting with abdominal and groin pain associated with chills and vomiting. Computerized tomography scan showed extensive cystic retroperitoneal lesion and ultrasound demonstrated “Dancing Filarial Sign.” Retroperitoneal filariasis can present without peripheral filarial signs. Hence, it should be considered in the differential diagnosis of acute abdominal pain of a patient who is originally from an endemic area.


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