A Rare Benign Pulmonary Neoplasm: A Case Report of Benign Pulmonary Papillary Adenoma

CHEST Journal ◽  
2017 ◽  
Vol 152 (4) ◽  
pp. A713
Author(s):  
Anna Kyu-K Khaing Chen ◽  
Michael Ayers ◽  
Ronald Evans
2016 ◽  
Vol 44 (6) ◽  
pp. 543-547 ◽  
Author(s):  
Amy Frey ◽  
Houda Alatassi ◽  
Tanya Ann Wiese ◽  
Mostafa Fraig ◽  
Xiu Yang

2015 ◽  
Vol 10 (1) ◽  
Author(s):  
Xu-Yong Lin ◽  
Qiang Han ◽  
En-Hua Wang ◽  
Yong Zhang

2014 ◽  
Vol 48 (1) ◽  
pp. 66 ◽  
Author(s):  
In Ho Choi ◽  
Joungho Han ◽  
Jung Won Moon ◽  
Yong Soo Choi ◽  
Kyung-Jong Lee

2020 ◽  
Vol 2020 ◽  
pp. 1-5
Author(s):  
Xingen Hu ◽  
Yi Chen ◽  
Guoqing Ru ◽  
Lili Yu

Papillary adenoma of the lung is a rather rare tumor. We will present a case of papillary adenoma in the lung with malignant transformation in a 65-year-old male patient. A high dense soft tissue mass was detected in the lateral segment of the right middle lobe by CT examination. Cytologically, the tumor contained the benign cells similar to normal alveolar epithelium and the malignant cells which were significantly enlarged and irregular, crowded, or overlapping. Immunohistochemical staining showed that the epithelial cells were diffusely positive for TTF-1, napsin-A, and CK7, but were negative for p63, p40, CK5/6, CgA, Syn, CD56, and TG. The Ki67 index was about 5%. All of these evidences indicated that it was a case of papillary adenoma with malignant transformation. Thus, it should be noted that more active treatment measures should be taken to treat pulmonary papillary adenoma.


2002 ◽  
Vol 38 (2) ◽  
pp. 125-127 ◽  
Author(s):  
Andrea Neusuess ◽  
Alexander Claviez ◽  
Thomas Schroeter ◽  
Dieter Harms ◽  
Meinolf Suttorp

1984 ◽  
Vol 45 (8) ◽  
pp. 1140-1145
Author(s):  
Yoshinori KUSAZIMA ◽  
Masayuki ITO ◽  
Masashi KATO ◽  
Ichiro KONISHI ◽  
Hideharu FUJITA ◽  
...  

2014 ◽  
Vol 3 (8) ◽  
pp. 2005-2007
Author(s):  
Shekappa C Malagimani ◽  
Jashvanth C T ◽  
Kasasomasekhar Kasasomasekhar ◽  
Ulhas Paga

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.


1985 ◽  
Vol 78 (4) ◽  
pp. 525-532
Author(s):  
Osamu Tanaka ◽  
Kazuhiro Ota ◽  
Tsutomu Hoshiya ◽  
Yukikazu Hyo ◽  
Takashi Matsunaga ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document