Abstract
Pulmonary Sclerosing Pneumocytoma (PSP) is considered as a benign tumor, although a few cases have been reported to have multiple lesions, recurrence, and even regional lymph nodes (LNs) metastasis. Here, we report a case of PSP with atypical histologic features and malignant biological behavior, and explore its molecular genetic changes. The 23-year-old male showed a 6.5-cm pulmonary nodule in the right middle lobe (RML) and enlarged media stinal LNs. He underwent thoracoscopic RML lobectomy, systematic LNs dissection, and mediastinal lymphadenectomy. The metastases to the cervical LNs and liver were detected in a short period and then resected. Postoperative pathological examination confirmed the diagnosis of PSP in all the lesions, based on the histological characteristics and immune phenotypes. Furthermore, whole-exome sequencing identified both AKT1 E17K somatic mutation and TP53 C176Y germline mutation in this case. Thus, we presented an extremely rare case of atypical PSP with rapid recurrence and multiply metastases, which can easily be misdiagnosed as primary lung cancer. In addition, PSP-specific AKT1 E17K somatic E17K somatic mutation accompanied with TP53 C176Y germline mutation may contribute to the malignant clinical course of this tumor.
Introduction
Pulmonary sclerosing pneumocytoma (PSP), formerly known as pulmonary sclerosing hemangioma, is a rare primary lung tumor originated from incompletely differentiated type II pneumocytes. Although PSP has some clinical and imaging characteristics for differentiation from similar lesions, these are not specific for diagnosis (, ). At present, its diagnosis still depends on surgical pathology. Occasionally, PSP may manifest as multiple lesions, recurrence, regional lymph nodes (LNs), or single organ metastasis, but is not likely to affect the prognosis. Therefore, PSP is considered as a benign or a low-grade malignant potential primary lung tumor (–). Herein, we report an extremely rare PSP case with atypical histological features, rapid recurrence and multiply metastases, and try to elucidate the molecular mechanism of the malignant progression through clinic pathological, Immunohistochemistry (IHC), and whole-exome sequencing (WES) data.
Case Presentation
Clinical History and Examination
A 23-year-old male was referred to Daping Hospital, Army Medical University for non-productive cough, chest distress, and fever for 1 month. He had no smoking and family disease history. Chest enhanced computed tomography (CT) scans confirmed a 6.5-cm pulmonary nodule in the right middle lobe (RML), with enlarged media stinal LN (Figures 1A,B). Positron-emission tomography (PET) showed increased uptake in the nodule and confirmed multiple media stinal LNs (Figures 1C,D), with no other areas of uptake. The blood examination showed that carcino embryonic antigen (CEA 8.4 ng/mL, the normal range 0.0–5.0 ng/mL) and CA153 (274.55 U/mL, the normal range 0.0–31.3 U/mL) were abnormal. The transthoracic radiology-guided biopsy considered epithelial tumor, preferred as adenocarcinoma. The patient underwent thoracoscopic RML lobectomy and systematic LNs dissection on July 27, 2018. Four months after the initial operation, the patient presented productive bloody cough. Chest enhanced CT scans showed an upper paratracheal LN measuring 3.2 × 2.2 cm. The second thoracoscopic media stinal lymphadenectomy was performed on November 20, 2018. On February 2019, 3 months after the second operation, neck-enhanced magnetic resonance imaging (MRI) showed an enlarged right supraclavicular LN measuring 5.4 × 3.8 cm (Figure 1E). The abdominal enhanced MRI showed a 1.5 × 1.2 cm nodule in the upper left lobe of the liver (Figure 1F). The patient underwent right neck mass resection on February 27, 2019, and laparoscopic liver mass resection on March 27, 2019.
Figure 1
Histopathologic Findings
A well-demarcated and circular mass, with grayish-white, slightly tough texture cut surface, was found in the RML (Figure 2A), 6 cm in diameter. Microscopically, the boundary between the tumor and the surrounding lung tissue was relatively clear except that a few minor infiltrative nodules were observed outside the main body of the tumor (Figure 2B). Solid cell area, papillary structure and sclerotic area composed of different proportion of surface epithelioid cells and polygonal stromal cells constituted the common mixed growth pattern of PSP (Figure 2C). Transition zone of solid and papillary pattern (Figure 2D), as well as the papillary structures in sclerosing background (Figure 2E) were observed, respectively. Focally in solid cell area, polygonal tumor cells distributed diffusely, with the increased cell density, and some pleomorphism and atypia appeared, but the mitosis was difficult to be found (Figure 2F). Focal tumor necrosis was noticed (Figure 2G). IHC analysis revealed that both the stromal cells and cuboidal surface cells showed positive for EMA and TTF-1 (Figure 2I), whereas only the surface cells expressed CK (Figure 2H), CEA, and Napsin A (Figure 2J). Most of the tumor cells were p53-positive (Figure 2K). The Ki-67 labeling index (LI) was about 5% (Figure 2L). PR was positive in polygonal stromal cells, while ER and Syn were positive in a few tumor cells. S-100, actin, desmin, HMB45, p63, and TFE3 were all negative. Double-labeling IHC showed CK7 and TTF-1 positive but PR negative in surface-lining epithelial cells, while CK7 negative but TTF-1 and PR positive in polygonal stromal cells (Figures 2M,N).
Figure 2
The histopathological and IHC staining of the resected specimens confirmed multiple organ metastasis of hilar, mediastinum (Figures 3A–E), cervical LNs, and liver (Figures 3F–J). Strikingly, the normal structures of LNs and the liver were partially destroyed. The polygonal tumor cells showed diffuse or patchy infiltration, increased pleomorphism and atypia, with intra-nuclear inclusions and tumor giant cells. Interstitial vascular hyperplasia and focal necrosis were easily identified. The metastatic tumors showed same immuno-phenotypes as the stromal cells of the primary lung tumor: diffuse expression of EMA, TTF-1(Figures 3C,H), PR (Figures 3D,I) and p53 (Figure 3J), but negative for CK7 and Napsin A (Figure 3C, red box). The Ki-67 LI of mediastinum LNs (Figure 3E) and liver metastasis were higher than that of the primary lesion (25 vs. 5%).
Figure 3
Identification of Oncogenic Mutations of AKT1 and TP53
Herein, we conducted a comprehensive examination of genetic alterations (somatic mutations) in formalin fixed paraffin-embedded (FFPE) samples from the primary and three metastatic lesions with matched adjacent normal tissue. High frequencies of AKT1 E17K mutations was detected in primary lung tumor, media stinal LN, cervical LN, and liver metastatic lesions (16.14, 16.83, 34.51, and 21.88%, respectively). TP53 C176Y mutations were identified in the primary lung lesion, mediastinal LN, cervical LN, and liver metastatic samples, with the frequencies of 42.41, 68.63, 72.84, and 50.52%, respectively. Interestingly, TP53 C176Y mutations were also detected in the paired normal tissue adjacent to the primary lung tumor (frequency 33.02%), suggesting that TP53 C176Y was a germline mutation in this patient (Table 1). This phenotype was further confirmed by the identification of the same mutation in the peripheral blood mononuclear cell (PBMC) sample.
Table 1
| Location | Sample No. | Chr | Type | Freq (%) | Gene | Mutation_c | Mutation_p | Type_specific |
|---|---|---|---|---|---|---|---|---|
| Lung | 1820610_3 | chr14 | SNV | 16.14 | AKT1 | c.49G>A | p.E17K | Missense |
| Mediastinal LNs | 1832384_3 | chr14 | SNV | 16.83 | AKT1 | c.49G>A | p.E17K | Missense |
| Cervical LNs | 1905401_2 | chr14 | SNV | 34.51 | AKT1 | c.49G>A | p.E17K | Missense |
| Liver | 1909075_2 | chr14 | SNV | 21.88 | AKT1 | c.49G>A | p.E17K | Missense |
| Normal tissue | 1820610_3a | chr17 | SNV | 33.02 | TP53 | c.527G>A | p.C176Y | Missense |
| Lung | 1820610_3 | chr17 | SNV | 42.41 | TP53 | c.527G>A | p.C176Y | Missense |
| Mediastinal LNs | 1832384_3 | chr17 | SNV | 68.63 | TP53 | c.527G>A | p.C176Y | Missense |
| Cervical LNs | 1905401_2 | chr17 | SNV | 72.84 | TP53 | c.527G>A | p.C176Y | Missense |
| Liver | 1909075_2 | chr17 | SNV | 50.52 | TP53 | c.527G>A | p.C176Y | Missense |
Clinical data, AKT1, and TP53 gene mutations in this atypical pulmonary sclerosing pneumocytomacase.
LNs, lymph nodes; Chr, chromosome; Freq, frequency; SNV, single nucleotide variation.
Clinical Outcome After the Fourth Operation
The patient received anti-estrogen therapy with medroxyprogesterone after the fourth operation, but the disease progressed rapidly. In May 2019, chest and abdominal enhanced CT scans showed multiple nodules in the right lung and multiple enlarged LNs in neck, jaw and right supraclavicular fossa. In September 2019, the patient felt that the neck mass was significantly larger than before. Chest and abdominal enhanced CT scans showed an enlarged mass in both lung hilum (5.8 × 5.4 cm) and right supraclavicular fossa (5.7 cm in maximum dimension), multiple nodules in the liver and left kidney, and thoracic 8th and 11th vertebral osteolytic bone destruction. The patient was then administered pembrolizumab treatment at 2 mg/kg intravenously every 3 weeks, combined with apatinib at 250 mg/day orally since October 2, 2019. As of January 10, 2021, after multiple cycles of combined treatment, the metastatic lesions were obviously reduced or in a stable state. The patient was in good mental state and had no significant change in weight.
Discussion
Due to the lack of specificity in clinical and imaging features, the diagnosis of PSP mainly depends on postoperative pathological examination. The diagnosis of typical PSP, characterized by two different cell components, four typical histological types, and immune phenotypes with specific features, is not difficult for pathologists (). However, some atypical cases may exhibit either different clinical behaviors from typical PSP, such as recurrence or metastasis, or confused histological characteristics, such as limited typical patterns, cytological atypia, and focal necrosis. These atypical cases could be misdiagnosed as papillary or solid subtype of lung adenocarcinoma and neuroendocrine tumor, especially in the case of needle biopsy or intraoperative frozen diagnosis (). In this case, the delayed diagnosis at biopsy was mainly attributed to the atypical phenomenon, including multiple LN metastases, papillary and solid growth pattern, cellular atypia, tumoral necrotic foci, and higher Ki-67 LI than that of ordinary PSP cases. Interestingly, only interstitial round cells, no surface cells, in LN and liver metastases of this case were observed. Consistently with other reports of the literature (, , , ), this morphology indicated that the stromal cells might play a critical role in malignant progression of PSP. Therefore, for accurate conclusions, we should comprehensively analyze the results of imaging, gross specimen performance, histopathology, IHC, and molecular detection, if necessary.
There are several points worth emphasizing on the pathological diagnosis. Firstly, PSP usually presents as an isolated, solid, and well-defined mass, which is different from the general changes of invasive adenocarcinoma. Secondly, we should deduce the basic structure for the diagnosis of PSP by observing the sections carefully and comprehensively: the papillary growth pattern and its diffuse distribution of interstitial cell components, as well as other histological patterns, such as solid cell area, intra-alveolar hemorrhage, and sclerotic changes. Thirdly, although there is no specific single antibody for diagnosis, establishing the diagnosis by the appropriate combination of antibodies and observing the obvious difference of immunophenotypes between epithelioid cells and stromal cells is imperative. Finally, for the atypical cases, the molecular pathologic findings are helpful for diagnosis. As in this case, we identified the AKT1 E17K point mutation through WES analysis, which is a relatively specific molecular feature of PSP (, ), but no other common driving gene mutations related to lung cancer were found, which played an important role in strengthening our confidence in the diagnosis of this atypical disease.
PSPs were mostly diagnosed in female patients (83.34%), aged 38–61 years (). The malignant progression and metastasis of PSP were extremely rare. The reported PSP patients with LN (, , , ) or organ metastases (, ) were mostly females, and only one male patient suffered from mediastinal LN metastasis (). Herein, we reported an extremely atypical case: a young male patient had been suffering from an aggressive PSP with multiple LN and organ metastases during 7 months after the resection of the primary lung lesion.
AKT1 E17K mutation, identified from all primary and metastatic lesions in this PSP case, were localized to the pleckstrin homology domain (PH domain), which is crucial for membrane localization and downstream activation of AKT1 () and is known to promote growth factor-independent cell proliferation (, ). However, though more than 40 PSP cases have been reported with AKT1 E17K mutation (, ), malignant progression has been rarely reported, which indicated that single E17K mutation on the PH domain of the AKT1 gene might not be sufficient to initiate the malignant transformation of the tumor. A 17-year-old girl suffering from multiple nodules in the right lung lobe diagnosed as PSP with both AKT1 E17K and BRAF V600E mutations (). The other PSP case with diffusely scattered nodules in the right lung, harbored AKT1 E17K and other 14 somatic gene mutations (). These indicated that the combination of AKT1 mutations with other oncogenes might accelerate the malignant progression of benign PSPs. For the first time, we reported a TP53 C176Y germline mutation, a likely pathogenic mutation according to the ClinVar and 1000Genomes database, in this extremely aggressive PSP case. Which consistent with the positive expression of the P53 mutant protein in the IHC assay. Therefore, rapid malignant progression leading to multiple metastases of this PSP case might be partially attributed to the combination of somatic AKT1 E17K mutation and germ line TP53 C176Y mutation. Germ line mutations of TP53 gene have been identified in 80% of patients with Li-Fraumeni syndrome (LFS), a cancer predisposition syndrome associated with high risks for a diverse spectrum of childhood- and adult-onset malignancies (). However, neither first- nor second-degree relatives had been diagnosed with any cancer or sarcoma, this patient does not meet the classic LFS diagnosis criteria ().
Conclusion
We report an extremely rare case of PSP, which showed obvious atypical features in histopathology and malignant biological behaviors, such as rapid recurrence and multiple metastases. Based on the results of WES, we speculated that the somatic AKT1 E17K and germline TP53 C176Y mutations might account for this malignant progression.
Funding
This work was supported by The National Natural Science Foundation of China (grant no. 81802781).
Publisher's Note
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Statements
Data availability statement
All data sets generated for this study are included in the article/supplementary material, further inquiries can be directed to the corresponding author.
Ethics statement
The studies involving human participants were reviewed and approved by the Clinical Ethics Committee of Daping Hospital, Army Medical University (Chongqing, China). The patients/participants provided their written informed consent to participate in this study. Written informed consent was obtained from the individual(s) for the publication of any potentially identifiable images or data included in this article.
Author contributions
QW and HX designed the study. MJ and XY investigated and provided the clinical data. QW, CL, LZ, and YY performed the molecular experiments. CM, CL, and PF performed the pathologic slides. QW and HX wrote the manuscript. ML, YH, and HX revised and edited the manuscript. All authors contributed to the article and approved the submitted version.
Conflict of interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
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Summary
Keywords
pulmonary sclerosing pneumocytoma, metastasis, AKT1, TP53, whole-exome sequencing
Citation
Wang Q, Lu C, Jiang M, Li M, Yang X, Zhang L, He Y, Mao C, Fu P, Yang Y and Xiao H (2021) Case Report and Literature Review: Pulmonary Sclerosing Pneumocytoma With Multiple Metastases Harboring AKT1 E17K Somatic Mutation and TP53 C176Y Germline Mutation. Front. Med. 8:655574. doi: 10.3389/fmed.2021.655574
Received
19 January 2021
Accepted
03 August 2021
Published
08 September 2021
Volume
8 - 2021
Edited by
Mattia Barbareschi, Azienda Provinciale per i Servizi Sanitari (APSS), Italy
Reviewed by
Alberto Cavazza, Azienda USL/IRCCS Reggio Emilia, Italy; Samir Abdullazade, University of Kiel, Germany
Updates
Copyright
© 2021 Wang, Lu, Jiang, Li, Yang, Zhang, He, Mao, Fu, Yang and Xiao.
This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Hualiang Xiao dpbl_xhl@126.com
†These authors have contributed equally to this work
This article was submitted to Pathology, a section of the journal Frontiers in Medicine
Disclaimer
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.