Solid placental transmogrification of the lung: A case report and literature review.
- Author:
Xue Mei HA
1
;
Yong Zheng YAO
2
;
Li Hua SUN
1
;
Chun Yan XIN
1
;
Yan XIONG
3
Author Information
1. Department of Pathology, Miyun District Hospital of Beijing, Beijing 101500, China.
2. Department of Thoracic Surgery, Miyun District Hospital of Beijing, Beijing 101500, China.
3. Department of Pathology, Peking University First Hospital, Beijing 100034, China.
- Publication Type:Journal Article
- Keywords:
Clinical pathology;
Differential diagnosis;
Lung disease;
Solid placental transmogrification of the lung
- MeSH:
Male;
Humans;
Female;
Pregnancy;
Middle Aged;
Hyperplasia/pathology*;
Placenta/pathology*;
Lung/pathology*;
Pulmonary Emphysema/surgery*;
Tomography, X-Ray Computed/methods*
- From:
Journal of Peking University(Health Sciences)
2023;55(2):357-361
- CountryChina
- Language:Chinese
-
Abstract:
Placental transmogrification of the lung (PTL) is a very rare benign lung lesion. There are only about 40 cases reported in the literature. The imaging and histological features of PTL cases in the publication are various, most of which are cystic and a few of which are solid. Being extremely rare, the solid PTL is unknown to major pathologists and surgeons. We reported a case of solid PTL in the anterior mediastinum. The patient was a 52-year-old male with no history of smoking and without symptoms. During physical examination, chest CT revealed a circular low-density lesion with a maximum diameter of 2.9 cm beside the spine in the posterior basal segment of the left lower lobe of the lung. The wedge resection was performed by video-assisted thoracoscopy. Grossly, a round nodule was located underneath the visceral pleura. It was about 3.0 cm×3.0 cm×1.6 cm and the cut surface was grey-red, soft and spongy. Microscopically, the nodule was constituted of papillare, which resembled placental villi at low magnification. The axis of papillae was edema, in which some mild round cells with clear cytoplasm and CD10 positive staining aggregated and transitioned to immature adipocytes and amorphous pink materials deposited with a few of inflammatory cells infiltration. The surface of papillae was covered with disconti-nuous alveolar epithelium. Combined with the typical morphology and immunohistochemical characteristics of CD10 positive, the diagnosis was PTL. The patient was followed up for 1 year without recurrence and discomfort. So far, the pathogenesis of PTL is unclear. The major hypotheses include hamartoma, variant of emphysema and clonal hyperplasia of stromal cells. Based on the study of our case and publication, we speculate that the hyperplasia of stromal cells located in the alveolar septa might be the first step to form the solid PTL. With the progression of the disease, a typical unilateral cystic nodule develops as a result of secondary cystic degeneration due to the occlusive valve effect. Surgery is the only option for diagnosis and treatment of PTL. The clinician should make an individualized operation plan according to the clinical manifestations, location and scope of the lesion, and preserve the surrounding normal lung tissue as much as possible while completely removing the lesion. There is a favorable prognosis.
