Case Reports in Oncological Medicine

Case Reports in Oncological Medicine / 2020 / Article

Case Report | Open Access

Volume 2020 |Article ID 9056209 | https://doi.org/10.1155/2020/9056209

Erdem Altunel, Aleksandr Perepletchikov, Olga Kozyreva, "Metastatic Syringocystadenocarcinoma Papilliferum: A Case Report, Tumor Genomic Profiling, and Literature Review", Case Reports in Oncological Medicine, vol. 2020, Article ID 9056209, 4 pages, 2020. https://doi.org/10.1155/2020/9056209

Metastatic Syringocystadenocarcinoma Papilliferum: A Case Report, Tumor Genomic Profiling, and Literature Review

Academic Editor: Raffaele Palmirotta
Received13 Dec 2019
Revised06 Jul 2020
Accepted30 Jul 2020
Published10 Aug 2020

Abstract

Syringocystadenocarcinoma papilliferum (SCACP) is an extremely rare cutaneous neoplasm of the apocrine or eccrine sweat glands. Solid and cystic glandular structures with cribriform and tubular architecture along with CK5/6, pankeratin and p63 immuno-profile set apart SCACP from other cutaneous malignancies. Wide local excision (WLE) has been the mainstay treatment for localized SCACP; however, no standard treatment has yet been established for unresectable or metastatic disease. Herein, we report a 74-year-old male with SCACP, who initially presented with a painful nodule on the upper back and later developed metastatic disease. He was treated with carboplatin and paclitaxel with concurrent intensity-modulated radiation therapy (IMRT), which resulted in disease stabilization for 12 months. Next generation sequencing (NGS) revealed a total of 18 genomic alterations associated with potential benefit from targeted therapeutics. PD-L1 expression was identified in 70% of tumor cells. These findings suggest that the opportunity of targeted therapeutics and immunotherapy exist as for metastatic SCACP. Reporting molecular profile of the rare tumors with no established standard treatment options should be encouraged.

1. Introduction

SCACP is an extremely rare cutaneous adnexal neoplasm, of which only less than 50 cases have been described in the literature since its first description in 1980 by Dissanayake et al. [1]. SCACP is originated from apocrine or eccrine sweat glands and often presents as a nodular mass in the scalp as well as other parts of the body [2]. Although its histopathologic features have been well described [35], the optimal treatment has not yet been established because of the rarity of the tumor. WLE has been the preferred treatment for localized SCACP [6]; however, there is no standard systemic therapy for the unresectable or metastatic disease. In addition, the genomic profile of SCACP has not yet been reported. Herein, we report a case of metastatic SCACP, its genomic profile, PD-L1 status, and response to the multimodal treatment.

2. Case Presentation

74-year-old otherwise healthy male presented with a painful nodule on the upper back. The lesion was initially diagnosed as a lipoma and surgically removed. However, six months after resection, the patient developed thoracic back pain. Thoracic MRI revealed an infiltrative mass of T3 to T5 vertebrae. A WLE with T3 to T5 laminectomy was performed, and the excision specimen was interpreted as squamous cell carcinoma. One year later, his back pain reemerged, and the patient developed bilateral lower extremity weakness, prompted a repeat MRI, which demonstrated soft tissue cystic mass at the T3 to T5 vertebral level invading the neural foramina bilaterally as well as an enlarged right axillary lymph node (Figure 1(a)). Fine needle aspiration of the lymph node showed a high-grade carcinoma showing papillary and tubular architectural features. The tumor cells were immunoreactive for high molecular weight keratin (CK5/6), wide spectrum cytokeratin, and p63 immuno-stains (Figure 1(b)). Taken together, the morphologic and immunophenotypic features supported the diagnosis of SCACP.

The patient was deemed not a surgical candidate and was treated with three cycles of carboplatin and paclitaxel with concurrent intensity-modulated radiation therapy (IMRT), which resulted in disease stabilization and significant improvement of his neurological symptoms. However, he developed right arm pain and weakness within a year of treatment, and the repeat imaging showed an increase in size of the right axillary lymph node and stable disease in his spine (Figure 2). The lymph node was resected and sent for the next generation sequencing (The FoundationOne assay interrogates 315 genes as well as introns of 28 genes involved in rearrangements), which revealed a total of 18 genomic alterations associated with potential benefit from targeted therapeutics (Table 1). PD-L1 expression was identified in 70% of tumor cells using Tumor Proportion Score (TPS). Patient was offered checkpoint inhibitor-based therapy that he declined.


GeneGene functionMutationMutation descriptionTargeted therapy

ARID2Activation of gene expression by nuclear receptorsQ725NonsenseNone
CDKN2ATumor suppressorp16INK4a Q50NonsensePalbociclib
ERBB4Cell proliferation and apoptosisR393WMissenseAfatinib, Erlotinib, Lapatinib
FAT1Inhibition of transcriptional activityG758fsFrameshiftNone
FGF10Regulation of cell growth, tumor growth and invasionAmplificationNone
FGFR1Regulation of the cell cycle and angiogenesisQ775NonsensePonatinib, Pazopanib
GNA11Modulation of transmembrane signaling systemR183CMissenseTrametinib
KDM5CControl gene expressionQ919NonsenseNone
MAGI2Inhibition of cell migration and proliferationQ117NonsenseNone
NFKBIATumor suppressorAmplificationNone
NOTCH1Regulation of cell fate, proliferation and apoptosis6181-1G >AIntronicNone
PIK3CARegulation of cell growth, proliferation, and survivalE453KMissenseEverolimus, Temsirolimus
RAC1Regulation of tumor angiogenesis, metastasis and cell growthP29SNonsenseNone
RICTOREncoding an mTOR-binding proteinAmplificationOmipalisib
SLIT2Tumor suppressorD1445HMissenseNone
TERTRegulation of chromosomal length124C >TIntronicNone
TP53Tumor suppressorQ331NonsenseAdavosertib
TP53Tumor suppressorQ375NonsenseAdavosertib

3. Discussion

SCACP is an extremely rare cutaneous neoplasm of the apocrine or eccrine sweat glands. Due to the rarity of this entity, clinical and pathologic diagnosis is challenging. However, solid and cystic glandular structures with cribriform and tubular architecture along with CK5/6, pankeratin, and p63 immuno-profile set apart SCACP from other cutaneous malignancies.

WLE has been the mainstay treatment for localized SCACP; however, high recurrence rate (30-40%) following surgery has been reported [4, 6]. For unresectable or metastatic disease, no standard treatment has yet been established. To date, there has been only one case reported, in which a cisplatin chemoradiation was delivered, and the patient was rendered disease free for 11 months [7]. Our patient achieved disease control for 12 months with carboplatin and paclitaxel concurrently with IMRT.

To determine potential therapeutic strategies, the molecular profile of the tumor was requested, which revealed 18 genomic alterations associated with potential clinical benefit (Table 1). Among these alterations, ERBB4 R293W has been previously observed in several cancers including malignant melanoma, which was found to be sensitive to the ERBB inhibitor, lapatinib in vitro [8]. Another genomic alteration which may indicate biological and therapeutic relevance is PIK3CA E453K [9]. PIK3CA activating mutations or amplification may predict sensitivity to inhibitors of PI3K or its downstream signaling pathway (the PI3K/Akt/mTOR pathway) [10]. Moreover, the impaired function of CDKN2A results in cell cycle dysregulation [11] and clinical benefit from CDK4/6 inhibitors has been shown in patients harboring CDKN2A alterations [12, 13]. Although these are potentially interesting findings, further studies will need to be performed to validate these genomic alterations.

Lastly, the efficacy of immunotherapy in the treatment of SCACP has not yet been demonstrated. To our knowledge, this is the first report of PD-L1 expression in SCACP, and the result suggests the possibility of using checkpoint inhibitors in this otherwise difficult to treat disease.

4. Conclusion

We report a case of metastatic SCACP, its histopathological and genomic characterization, and response to the combined modality of treatment. The opportunity of targeted therapeutics and immunotherapy exist as for metastatic SCACP. Reporting molecular profile of the rare tumors with no established standard treatment options should be encouraged.

Conflicts of Interest

The authors declare that they have no conflicts of interest.

References

  1. R. V. P. Dissanayake and R. Salm, “Sweat-gland carcinomas: prognosis related to histological type,” Histopathology, vol. 4, no. 4, pp. 445–466, 1980. View at: Publisher Site | Google Scholar
  2. V. Parekh, C. E. Guerrero, C. F. Knapp, C. A. Elmets, and K. M. McKay, “A Histological Snapshot of Hypothetical Multistep Progression From Nevus Sebaceus to Invasive Syringocystadenocarcinoma Papilliferum,” The American Journal of Dermatopathology, vol. 38, no. 1, pp. 56–62, 2016. View at: Publisher Site | Google Scholar
  3. N. Iga, H. Fujii, T. Miyake, M. Ehara, and S. Kore-eda, “Syringocystadenocarcinoma Papilliferum in the perianal area,” Case Reports in Dermatology, vol. 7, no. 2, pp. 84–89, 2015. View at: Publisher Site | Google Scholar
  4. Y. Zhang, Y. Y. Kong, X. Cai, X. X. Shen, and J. C. Kong, “Syringocystadenocarcinoma papilliferum: Clinicopathologic analysis of 10 cases,” Journal of Cutaneous Pathology, vol. 44, no. 6, pp. 538–543, 2017. View at: Publisher Site | Google Scholar
  5. B. Paradiso, E. Bianchini, P. Cifelli, L. Cavazzini, and G. Lanza, “A new case of syringocystadenocarcinoma papilliferum: a rare pathology for a wide-ranging comprehension,” Case Reports in Medicine, vol. 2014, Article ID 453874, 8 pages, 2014. View at: Publisher Site | Google Scholar
  6. H. Arslan, M. Diyarbakrl, Ş. Batur, and C. Demirkesen, “Syringocystadenocarcinoma Papilliferum With Squamous Cell Carcinoma Differentiation and With Locoregional Metastasis,” The Journal of Craniofacial Surgery, vol. 24, no. 1, pp. e38–e40, 2013. View at: Publisher Site | Google Scholar
  7. P. B. Rao, S. Ghosh, M. Mohapatra et al., “Chemoradiotherapy in a case of malignant syringocystadenocarcinoma papilliferum of vulva with locoregional failure,” Case Reports in Oncological Medicine, vol. 2015, Article ID 638294, 4 pages, 2015. View at: Publisher Site | Google Scholar
  8. T. D. Prickett, N. S. Agrawal, X. Wei et al., “Analysis of the tyrosine kinome in melanoma reveals recurrent mutations in ERBB4,” Nature Genetics, vol. 41, no. 10, pp. 1127–1132, 2009. View at: Publisher Site | Google Scholar
  9. T. Ikenoue, F. Kanai, Y. Hikiba et al., “Functional analysis of PIK3CA gene mutations in human colorectal Cancer,” Cancer Research, vol. 65, no. 11, pp. 4562–4567, 2005. View at: Publisher Site | Google Scholar
  10. F. Janku, A. M. Tsimberidou, I. Garrido-Laguna et al., “PIK3CA Mutations in Patients with Advanced Cancers Treated with PI3K/AKT/mTOR Axis Inhibitors,” Molecular Cancer Therapeutics, vol. 10, no. 3, pp. 558–565, 2011. View at: Publisher Site | Google Scholar
  11. J. Monzon, L. Liu, H. Brill et al., “CDKN2A mutations in multiple primary melanomas,” New England Journal of Medicine, vol. 338, no. 13, pp. 879–887, 1998. View at: Publisher Site | Google Scholar
  12. S. K. Pal, S. M. Ali, J. Ross, T. K. Choueiri, and J. H. Chung, “Exceptional response to palbociclib in metastatic collecting duct carcinoma bearing a CDKN2A Homozygous deletion,” JCO Precision Oncology, vol. 1, pp. 1–5, 2017. View at: Publisher Site | Google Scholar
  13. J. A. Elvin, L. M. Gay, R. Ort et al., “Clinical benefit in response to Palbociclib treatment in refractory uterine Leiomyosarcomas with a common CDKN2A alteration,” The Oncologist, vol. 22, no. 4, pp. 416–421, 2017. View at: Publisher Site | Google Scholar

Copyright © 2020 Erdem Altunel et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.


More related articles

 PDF Download Citation Citation
 Download other formatsMore
 Order printed copiesOrder
Views384
Downloads371
Citations

Related articles

Article of the Year Award: Outstanding research contributions of 2020, as selected by our Chief Editors. Read the winning articles.