scholarly journals An unexpected zoonosis: pulmonary dirofilaria infection mimicking pulmonary neoplasm

2019 ◽  
Vol 7 (8) ◽  
Author(s):  
Gordon Maxwell ◽  
Jaideep Sood ◽  
Stephen Allpress
Keyword(s):  
1983 ◽  
Vol 3 (1) ◽  
pp. 114-117
Author(s):  
Suman Vardan ◽  
Kumar Ashutosh ◽  
Sakti Mookherjee

1964 ◽  
Vol 8 (3) ◽  
pp. 259-265 ◽  
Author(s):  
J. E. Blundell ◽  
J. T. Wright

2005 ◽  
Vol 100 ◽  
pp. S217
Author(s):  
Herve C. Boucard ◽  
Shahida Ahmed ◽  
Sima Vossough

1977 ◽  
Vol 13 (3) ◽  
pp. 451-469 ◽  
Author(s):  
Katharine R. Boucot ◽  
Herbert Seidman ◽  
William Weiss

2006 ◽  
Vol 53 (6) ◽  
pp. 288-292 ◽  
Author(s):  
J. S. Munday ◽  
S. E. Boston ◽  
M. C. Owen ◽  
A. F. French ◽  
D. Aberdein

2020 ◽  
Author(s):  
leilei shen ◽  
Jixing LIN ◽  
Zhipeng REN ◽  
Bailin WANG ◽  
You Liu ◽  
...  

Abstract Background: Clear cell tumor of the lung (CCTL) is a rare and mostly benign pulmonary neoplasm arising from perivascular epithelioid cells. Only about 100 cases have been reported and half of them were in China. Limited details about CCTL often cause diagnostic or therapeutic problems. Case presentation: We describe a case of 28-year-old woman with gradually increased and enlarged multiple nodules in the left lower lobe. The patient underwent a fine-needle aspiration biopsy and was considered as CCTL. A left lower lobectomy and mediastinal lymph node dissection was performed. The gradual changes in size (1.4 cm to 2.8 cm) and quantity (10 to 49) of CCTL in this case was the biggest difference from previously reported cases. Conclusions: CCTL is a very uncommon and mostly benign PEComatous tumor with no specific morphologic features. We present a case of CCTL with multiplicity and rapid growth, which may indicate its aggressive nature. The accumulation of similar cases will help clarify its exact disease nature and to improve our understanding of such tumor.


2020 ◽  
Vol 90 (3) ◽  
Author(s):  
Christos Kakos ◽  
Savvas Lampridis ◽  
Georgios Geropoulos ◽  
Reena Khiroya ◽  
Achilleas Antonopoulos ◽  
...  

Cystic fibrohistiocytic tumour of the lung is a very rare pathological entity that occurs either as a primary pulmonary neoplasm or as a metastasis from skin lesions called cellular fibrous histiocytomas. Herein, we present the case of a 19-year old man with a history of recurrent pneumothoraces who was managed surgically and was eventually diagnosed with cystic fibrohistiocytic tumour of the lung. Clinicians should include this disease in the differential diagnosis of pulmonary cystic lesions and be aware of its association with cellular fibrous histiocytoma. Reporting of more cases is warranted to further elucidate the natural course of the disease and optimise its management.


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