Discussion
Diagnosis With Brief Discussion
- Diagnosis
- Pulmonary sclerosing pneumocytoma
- Radiologic Findings
- Chest radiograph (Fig 1) shows a well-defined small nodule in right lower lung field.
Axial chest CT images (Fig 2-4) show 2.8 cm oval, well-defined enhancing nodule in RLL. The contrast-enhanced axial image shows a subtle enhancing high attenuated rim, defined as the 'marginal pseudocapsule sign'. Enhancing vascular structure is observed at the edge of the nodule extending toward the hilum of the lung. It was defined as the 'overlying vessel sign'. The axial CT image with lung window setting shows a mass with surrounding GGO, defined as the 'halo sign'. Compared with previous CT obtained 5 years ago (Fig 5, 6), the tumor shows slow growth in size.
The patient underwent core-needle biopsy for the mass. The pathological diagnosis was sclerosing pneumocytoma.
- Brief Review
- Pulmonary sclerosing pneumocytomas (PSP), previously known as pulmonary sclerosing hemangiomas (PSH), also known as are rare benign neoplasms of the lung. It typically presents in middle age (30-50 years of age). There is a recognized female predilection. Most patients are asymptomatic. Symptoms if present will include hemoptysis, cough, chest pain, dyspnea, and pleurisy. The lesions range from 0.8 to 8.2 cm in diameter, but most are less than 3.5 cm in diameter.
Histologically, the essence is proliferation of type 2 pneumocytes, and a pneumocytoma consists of four major histologic components: solid, papillary, sclerotic, and hemangiomatous.
PSP typically presents on chest radiograph as a solitary, well-defined oval to rounded nodular lesion. Occasionally may contain areas of calcification and air-meniscus sign.
CT shows a smoothly marginated, homogeneously well-enhanced, round or oval nodule/mass with foci of calcification and air meniscus. Differentiation from lung cancer may be difficult on CT. A recent study reported that most patients had a single lesion (92.1%), smooth boundary (65.8%), and oval shape (65.8%), with a mean diameter of 2.27 cm. CT signs included marginal pseudocapsule (50%), overlying vessel (26.3%), air gap (2.6%), and halo sign (17.1%).
PSP can be very challenging to diagnose in frozen sections, small biopsies, and cytology where they can easily be mistaken for adenocarcinoma or carcinoid tumors. These tumors typically have a benign clinical course, with metastasis being exceedingly rare. Treatment of PSP involves surgical resection and the prognosis is favorable.
- References
- 1. Shin SY, Kim MY, Oh SY, et al. Pulmonary sclerosing pneumocytoma of the lung: CT characteristics in a large series of a tertiary referral center. Medicine (Baltimore). 2015 Jan;94(4):e498.
2. Lim JH, Lee N, Choi DW, et al. Pulmonary sclerosing pneumocytoma mimicking lung cancer: Case report and review of the literature. Thorac Cancer. 2016 Jul;7(4):508-11.
3. Furuya K, Yasumori K, Takeo S, et al. Lung CT: Part 1, Mimickers of lung cancer--spectrum of CT findings with pathologic correlation. AJR 2012; 199:W454?W463
4. Cheung YC, Ng SH, Chang JWC, et al. Histopathological and CT features of pulmonary sclerosing haemangiomas. Clin Radiol 2003;58:630e5.
- Please refer to
- Case 1023 Case 730 Case 540 Case 401 Case 318 Case 268 Case 168 Case 148 Case 142
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- Keywords
- Lung, Pulmonary sclerosing pneumocytoma, Marginal pseudocapsule, Overlying vessel sign, Halo sign, Sclerosing Hemangioma