This case produces two interesting findings as following. Firstly, bronchial papilloma and PSH are rare tumors while the description of a new case enhances the understanding of these diseases. Secondly, relative to the previous literature, co-occurrence of bronchial papilloma and PSH in a middle aged male is rare.
It is usually presented as an endobronchial mass in the segmental bronchi when bronchial papilloma occurs in the tracheobronchial tree, which has been diagnosed by bronchial biopsy of the specimen (Aida et al. 2008). To date, the major issue in bronchial papilloma is that both the clinical presentation and the analysis of the literature show protean symptoms and chest radiographs presentation (Yıldırım et al. 2015; Aida et al. 2008; Paganin et al. 2009). Many patients of bronchial papilloma have symptoms such as cough, dyspnea, wheezing, hemoptysis, or recurrent pneumonia for bronchial obstruction and lobar collapse, and their radiological findings show bronchiectasis or bronchial stenotic change that may be secondary to the recurrent pneumonia (Yıldırım et al. 2015; Paganin et al. 2009). Our patient has productive cough and fever, but this symptom has been considered as the clinical presentation of lung abscess for the abnormal shadow on the patient’s chest radiograph.
Bronchial papilloma is seen more frequently in men and generally appears in the age range of 50–70 years. The treatment methods for bronchial papilloma, such as endoscopic resection or surgical resection, are still controversial for the pathological examination of the whole papilloma can be prevented by laser irradiation while the extent of surgical resection is also a serious consideration, because these benign tumors are mostly located at the main bronchus or orifice of the lobar bronchus (Yıldırım et al. 2015; Harris and Chalhoub 2011; Paganin et al. 2009). In this case of a 48-year old man, for it is complicated with suspicious lung abscess and the patient’s own choice, the lobectomy has been performed instead of the endoscopic intervention (Paganin et al. 2009).
Of particular interest, after surgical resection, the lesion of the right upper lobe in our case is a PSH proved by histopathological examination. As widely known, PSH is a rare benign tumor of the lung, which occurs predominantly in middle aged women (Guerra-Gutiérrez et al. 2007). In most cases, PSH is detected by chance because it is generally asymptomatic as is the case in our patient who is a 48-years-old man with fever and cough, and found by surgical resection for the treatment of another rare benign tumor. Therefore, it is important that the diagnosis of PSH is preoperatively established whenever possible because a limited, but complete, resection of the lesion is the treatment of choice. PSH has the characteristics of a benign pulmonary mass, including a well-defined round or oval mass on radiography, a well-circumscribed lesion with marked contrast enhancement on CT and calcification might be detected in the minority of cases as found in our case (Shin et al. 2014; Zhu et al. 2010). We here report the case of a PSH radiologically presenting as a cystic lesion that has been indicated by Qian et al. (2012), and suggest the existence of a connection between the lesion and bronchi which caused the symptom of productive cough.
Our immunohistochemical results have suggested that the tumor cells stained positively for TTF-1, EMA, CK7, cytokeratin and CD31 that indicate the tumor originates from the epithelium, especially from type-II pneumocytes or Clara cells, but not from endothelium and the mass was decided as a sclerosis haemangioma of lung. As noted above, bronchial papilloma and PSH have been reported respectively in the literature. To the best of our knowledge, we introduce the case of a patient with the diagnosis of bronchial papilloma and PSH.
Although PSH has not been previously associated with bronchial papilloma, cases of PSH co-occurring with myomas, or with thyroid and kidney cysts have been reported in the literature, and these could indicate that PSH is yet another of the malformations that might be present in bronchial papilloma while other reports also have revealed that PSH has been found in association with Cowden syndrome or Lynch syndrome (Guerra-Gutiérrez et al. 2007; Schiergens et al. 2011). However, the pathophysiology of the association between bronchial papilloma and PSH is unclear.
In conclusion, this is a reported case of PSH in a male suffering from bronchial papilloma which is the exceptional concurrence of these two extremely infrequent events. This case highlights the fact that even though some of these lesions may have a low prevalence, they may be included in the differential diagnosis of solitary lung lesions. Nonetheless, the low prevalence of both diseases has meant that it has not been possible to explore the depth of association between them.
