Skip to main content
Log in

Primary intraosseous papillary intralymphatic angioendothelioma of the distal femoral epiphysis: a case report with literature review

  • Case Report
  • Published:
Skeletal Radiology Aims and scope Submit manuscript

Abstract

Introduction

Papillary intralymphatic angioendothelioma (PILA) is an exceptionally rare metastasizing soft tissue tumor. It tends to arise in the subcutaneous tissues of distal extremities in children. Only four intraosseous PILA cases have been reported until now in English language literature.

Case report

We present a case of PILA arising in the distal femoral epiphysis of a 50-year-old female patient. It started as a relentless pain in her left knee. A plain radiography revealed a radiolucent area in the left internal femoral condyle. Computerized tomography revealed a 1-cm lytic lesion with a sclerotic rim. Magnetic resonance images showed a significant bone marrow edema signal focused on a 1-cm subchondral lesion suggestive of an intraarticular osteoid osteoma. Histologically, the tumor contained vascular channels covered by a single endothelial layer with intraluminal papillary endothelial structures lined with hobnail cells. Immunohistochemically, the cells were positive for ERG, CD31, and D2-40. The tumor underwent cryoablation and 6 months later, after local recurrence or tumor persistence, a wide tumor resection was referred. After 7 years of follow-up, the patient displayed neither local recurrence nor distant metastases.

Conclusion

Primary intraosseous PILAs are exceedingly rare tumors that should be considered in the differential diagnosis of vascular bone tumors.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2

Similar content being viewed by others

References

  1. Dabska M. Malignant endovascular papillary angioendothelioma of the skin in childhood. Clinicopathologic study of 6 cases. Cancer. 1969;24(3):503–10. https://doi.org/10.1002/1097-0142(196909)24:3%3c503::AID-CNCR2820240311%3e3.0.CO;2-L.

    Article  CAS  PubMed  Google Scholar 

  2. Fanburg-Smith JC, Michal M, Partanen TA, Alitalo K, Miettinen M. Papillary intralymphatic angioendothelioma (PILA): a report of twelve cases of a distinctive vascular tumor with phenotypic features of lymphatic vessels. Am J Surg Pathol. 1999;23(9):1004–10. https://doi.org/10.1097/00000478-199909000-00002.

    Article  CAS  PubMed  Google Scholar 

  3. Fanburg-Smith J. Papillary intralymphatic angioendothelioma. In: WHO classification of tumours of soft tissue and bone. 5th. Agency for Research on Cancer; 2020:161–162.

  4. Goldblum J, Folpe A, Weiss S. Hemangioendothelioma: vascular tumors of intermediate malignancy. In: Enzinger & Weiss’s soft tissue tumors. 7th ed. Elsevier; 2020:757–784.

  5. McCarthy EF, Lietman S, Argani P, Frassica FJ. Endovascular papillary angioendothelioma (Dabska tumor) of bone. Skeletal Radiol. 1999;28(2):100–3. https://doi.org/10.1007/s002560050482.

    Article  CAS  PubMed  Google Scholar 

  6. Nakayama T, Nishino M, Takasu K, Hayakawa K, Toguchida J, Tanaka C. Endovascular papillary angioendothelioma (Dabska tumor) of bone. Orthopedics. 2004;27(3):327–8. https://doi.org/10.3928/0147-7447-20040301-19.

    Article  PubMed  Google Scholar 

  7. Bin LI, Li Y, Tian Xiao-ying, Li Zhi. Unusual multifocal intraosseous papillary intralymphatic angioendothelioma (Dabska tumor) of facial bones: a case report and review of literature. Diagn Pathol. 2013;8:160. https://doi.org/10.1186/1746-1596-8-160.

    Article  Google Scholar 

  8. Gambarotti M, Righi A, Sbaraglia M, et al. Intraosseous papillary intralymphatic angioendothelioma (PILA): one new case and review of the literature. Clin Sarcoma Res. 2018;8:1. https://doi.org/10.1186/s13569-018-0087-9.

    Article  PubMed  PubMed Central  Google Scholar 

  9. Takaoka K, Sakurai K, Noguchi K, Hashitani S, Urade M. Endovascular papillary angioendothelioma (Dabska tumor) of the tongue: report of a case. J Oral Pathol Med. 2003;32(8):492–5. https://doi.org/10.1034/j.1600-0714.2003.00120.x.

    Article  PubMed  Google Scholar 

  10. Katz JA, Mahoney DH, Shukla LW, Smith CW, Gresik MV, Hawkins HK. Endovascular papillary angioendothelioma in the spleen. Pediatr Pathol. 1988;8(2):185–93. https://doi.org/10.3109/15513818809022296.

    Article  CAS  PubMed  Google Scholar 

  11. Schultheis AM, Sandmann M, Steurer S. Strong ERG positivity in papillary intralymphatic angioendothelioma of the testis of a 24-year-old male: a case report. Case Rep Pathol. 2013;2013:531479. https://doi.org/10.1155/2013/531479.

    Article  PubMed  PubMed Central  Google Scholar 

  12. Qian T, Wu Z, Lu T. An extremely rare malignant Dabska tumour in right atria for a premature neonate. Eur Heart J Case Rep. 2022;6(1):ytab510. https://doi.org/10.1093/ehjcr/ytab510.

    Article  PubMed  Google Scholar 

  13. Manfrini M, Fiscina S, Righi A, Montes JM, Vanel D. Multiple or metastatic clear cell chondrosarcoma: a case report. Clin Sarcoma Res. 2014;4(1):12. https://doi.org/10.1186/2045-3329-4-12.

    Article  PubMed  PubMed Central  Google Scholar 

  14. Georgakopoulou D, Anastasilakis AD, Makras P. Adult Langerhans cell histiocytosis and the skeleton. J Clin Med. 2022;11(4):909. https://doi.org/10.3390/jcm11040909.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  15. Argani P, Athanasian E. Malignant endovascular papillary angioendothelioma (Dabska tumor) arising within a deep intramuscular hemangioma. Arch Pathol Lab Med. 1997;121(9):992–5.

    CAS  PubMed  Google Scholar 

  16. Antosz Z, Zaniewski M, Kostecki J, Poreba R. Angiosarcoma arising within a malignant endovascular papillary angioendothelioma (Dabska tumor). Neuro Endocrinol Lett. 2010;31(4):454–6.

    PubMed  Google Scholar 

  17. Gherman CD, Fodor D. Epithelioid hemangioendothelioma of the forearm with radius involvement. Case report Diagn Pathol. 2011;6(1):120. https://doi.org/10.1186/1746-1596-6-120.

    Article  PubMed  Google Scholar 

  18. Jung TY, Jung S, Lee MC, Kim IY, Kang SS, Kim SH. Papillary endothelial hyperplasia associated with repeated bleeding. Br J Neurosurg. 2005;19(5):428–31. https://doi.org/10.1080/02688690500390383.

    Article  PubMed  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to E. M. Pena-Burgos.

Ethics declarations

Conflict of interest

The authors declare no competing interests.

Additional information

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Pozo-Kreilinger, J.J., Pena-Burgos, E.M., Ortiz-Cruz, E.J. et al. Primary intraosseous papillary intralymphatic angioendothelioma of the distal femoral epiphysis: a case report with literature review. Skeletal Radiol (2024). https://doi.org/10.1007/s00256-024-04674-8

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1007/s00256-024-04674-8

Keywords

Navigation