全部 标题 作者
关键词 摘要

OALib Journal期刊
ISSN: 2333-9721
费用:99美元

查看量下载量

Synchronous Papillary Thyroid Carcinoma and Renal Epithelioid Angiomyolipoma with Hepatic Metastasis or Concurrence: A Clinicopathological Characteristics and Outcome

DOI: 10.4236/oalib.1109736, PP. 1-11

Subject Areas: Oncology, Diagnostics, Pathology

Keywords: EAML, Synchronous, Kidney

Full-Text   Cite this paper   Add to My Lib

Abstract

The epithelioid angiomyolipoma (EAML) is a variant of angiomyolipoma with predominant epithelioid component which has a potentially malignant behavior. We report a 40-year-old woman with the synchronous renal and hepatic epithelioid angiomyolipoma with preoperative papillary thyroid carcinoma. She had been operated to remove the tumors in her liver and kidney. The histopathological and immunohistochemical results of surgical specimens were concordant with epithelioid angiomyolipoma. Her thyroid carcinoma is still followed up to evaluate. After surgery she had not received any adjuvant therapy. Currently, after 8 months of treatment, she has not appeared with recurrent lesions.

Cite this paper

Le, D. T. , Nguye, T. V. , Do, T. A. , Vu, C. T. , Pham, K. H. , Dao, T. V. and Nguyen, C. V. (2023). Synchronous Papillary Thyroid Carcinoma and Renal Epithelioid Angiomyolipoma with Hepatic Metastasis or Concurrence: A Clinicopathological Characteristics and Outcome. Open Access Library Journal, 10, e9736. doi: http://dx.doi.org/10.4236/oalib.1109736.

References

[1]  Mai, K.T., Perkins, D.G. and Collins, J.P. (1996) Epithelioid Cell Variant of Renal Angiomyolipoma. Histopathology, 28, 277-280. https://doi.org/10.1046/j.1365-2559.1996.d01-421.x
[2]  Aydin, H., Magi-Galluzzi, C., Lane, B.R., Sercia, L., Lopez, J.I., Rini, B.I., et al. (2009) Renal Angiomyolipoma: Clinicopathologic Study of 194 Cases with Emphasis on the Epithelioid Histology and Tuberous Sclerosis Association. The American Journal of Surgical Pathology, 33, 289-297. https://doi.org/10.1097/PAS.0b013e31817ed7a6
[3]  He, W., Cheville, J.C., Sadow, P.M., Gopalan, A., Fine, S.W., Al-Ahmadie, H.A., et al. (2013) Epithelioid Angiomyolipoma of the Kidney: Pathological Features and Clinical Outcome in a Series of Consecutively Resected Tumors. Modern Pathology, 26, 1355-1364. https://doi.org/10.1038/modpathol.2013.72
[4]  WHO (2022) Classification of Tumours of the Urinary System and Male Genital Organs. 5th Edition, International Agency for Research on Cancer, Lyon, France.
[5]  Lane, B.R., Aydin, H., Danforth, T.L., Zhou, M., Remer, E.M., Novick, A.C., et al. (2008) Clinical Correlates of Renal Angiomyolipoma Subtypes in 209 Patients: Classic, Fat Poor, Tuberous Sclerosis Associated and Epithelioid. Journal of Urology, 180, 836-843. https://doi.org/10.1016/j.juro.2008.05.041
[6]  Brimo, F., Robinson, B., Guo, C., Zhou, M., Latour, M. and Epstein, J.I. (2010) Renal Epithelioid Angiomyolipoma with Atypia: A Series of 40 Cases with Emphasis on Clinicopathologic Prognostic Indicators of Malignancy. The American Journal of Surgical Pathology, 34, 715-722. https://doi.org/10.1097/PAS.0b013e3181d90370
[7]  Lei, J.H., Liu, L.R., Wei, Q., Song, T.R., Lu, Y., Yuan, H.C., et al. (2015) A Four-Year Follow-Up Study of Renal Epithelioid Angiomyolipoma: A Multi-Center Experience and Literature Review. Scientific Reports, 5, Article No. 10030. https://doi.org/10.1038/srep10030
[8]  Konosu-Fukaya, S. (2014) Renal Epithelioid Angiomyolipoma with Malignant Features: Histological Evaluation and Novel Immunohistochemical Findings. Pathology International, 64, 133-141. https://doi.org/10.1111/pin.12142
[9]  Svec, A. and Velenská, Z. (2005) Renal Epithelioid Angiomyolipoma—A Close Mimic of Renal Cell Carcinoma. Report of a Case and Review of the Literature. Pathology—Research and Practice, 200, 851-856. https://doi.org/10.1016/j.prp.2004.09.004
[10]  Huang, K.H., Huang, C.Y., Chung, S.D., Pu, Y.S., Shun, C.T. and Chen, J. (2007) Malignant Epithelioid Angiomyolipoma of the Kidney. Journal of the Formosan Medical Association, 106, S51-S54. https://doi.org/10.1016/S0929-6646(09)60353-3
[11]  Lau, S.K., Marchevsky, A.M., Jr, R.J.M. and Luthringer, D.J. (2003) Malignant Monotypic Epithelioid Angiomyolipoma of the Retroperitoneum. International Journal of Surgical Pathology, 11, 223-228. https://doi.org/10.1177/106689690301100313
[12]  Yang, J.W., Liang, C. and Yang, L. (2022) Advancements in the Diagnosis and Treatment of Renal Epithelioid Angiomyolipoma: A Narrative Review. The Kaohsiung Journal of Medical Sciences, 38, 925-932. https://doi.org/10.1002/kjm2.12586
[13]  Saleeb, R.M., Srigley, J.R., Sweet, J., Douce, C., Royal, V., Chen, Y.B., et al. (2017) Melanotic MiT Family Translocation Neoplasms: Expanding the Clinical and Molecular Spectrum of This Unique Entity of Tumors. Pathology-Research and Practice, 213, 1412-1418. https://doi.org/10.1016/j.prp.2017.08.004
[14]  Bonetti, F., Pea, M., Martignoni, G. and Zamboni, G. (1992) PEC and Sugar. The American Journal of Surgical Pathology, 16, 307-308. https://doi.org/10.1097/00000478-199203000-00013
[15]  Martignoni, G., Pea, M., Reghellin, D., Zamboni, G. and Bonetti, F. (2008) Pecomas: The Past, the Present and the Future. Virchows Archiv, 452, 119-132. https://doi.org/10.1007/s00428-007-0509-1
[16]  Hassan, M., El-Hefnawy, A.S., Elshal, A.M., Mosbah, A., El-Baz, M. and Shaaban, A. (2014) Renal Epithelioid Angiomyolipoma: A Rare Variant with Unusual Behavior. International Urology and Nephrology, 46, 317-322. https://doi.org/10.1007/s11255-013-0510-3
[17]  Martignoni, G., Pea, M., Bonetti, F., Zamboni, G., Carbonara, C., Longa, L., et al. (1998) Carcinomalike Monotypic Epithelioid Angiomyolipoma in Patients without Evidence of Tuberous Sclerosis: A Clinicopathologic and Genetic Study. The American Journal of Surgical Pathology, 22, 663-672. https://doi.org/10.1097/00000478-199806000-00003
[18]  Takahashi, N., Kitahara, R., Hishimoto, Y., Ohguro, A., Hashimoto, Y. and Suzuki, T. (2003) Malignant Transformation of Renal Angiomyolipoma. International Journal of Urology, 10, 271-273. https://doi.org/10.1046/j.1442-2042.2003.00620.x
[19]  Zhong, D.R. and Ji, X.L. (2000) Hepatic Angiomyolipoma-Misdiagnosis as Hepatocellular Carcinoma: A Report of 14 Cases. World Journal of Gastroenterology, 6, 608-612.
[20]  Nguyen, T., Gorman, B., Shields, D. and Goodman, Z. (2008) Malignant Hepatic Angiomyolipoma: Report of a Case and Review of Literature. The American Journal of Surgical Pathology, 32, 793-798. https://doi.org/10.1097/PAS.0b013e3181607349
[21]  Makhlouf, H.R., Remotti, H.E. and Ishak, K.G. (2002) Expression of KIT (CD117) in Angiomyolipoma. The American Journal of Surgical Pathology, 26, 493-497. https://doi.org/10.1097/00000478-200204000-00012
[22]  Nese, N., Martignoni, G., Fletcher, C.D., Gupta, R., Pan, C.C., Kim, H.L., et al. (2011) Pure Epithelioid PEComas (So-Called Epithelioid Angiomyolipoma) of the Kidney: A Clinicopathologic Study of 41 Cases: Detailed Assessment of Morphology and Risk Stratification. The American Journal of Surgical Pathology, 35, 161-176. https://doi.org/10.1097/PAS.0b013e318206f2a9
[23]  Bi, X.G., Guo, L., Wang, X.L., Wei, Q., Du, Q., Jiang, W.H., et al. (2017) Distinct Subcellular Localization of E-Cadherin between Epithelioid Angiomyolipoma and Triphasic Angiomyolipoma: A Preliminary Case-Control Study. Oncology Letters, 14, 695-704. https://doi.org/10.3892/ol.2017.6272
[24]  Zhu, Q.Q., Niu, Z.F., Yu, F.D., Wu, Y. and Wang, G.B. (2021) Epithelioid Angiomyolipoma of the Pancreas: A Case Report and Review of the Literature. World Journal Clinical Cases, 9, 1931-1939. https://doi.org/10.12998/wjcc.v9.i8.1931
[25]  Marcuzzia, A., Haiderb, E.A. and Salmi, I.S.A. (2018) Hepatic Epithelioid Angiomyolipoma with Renal Metastasis: Radiologic-Pathologic Correlation. Radiology Case Reports, 13, 829-833. https://doi.org/10.1016/j.radcr.2018.05.007
[26]  Azevedo, A.S.D. and Simão, N.M.M.S. (2015) Multicentric Angiomyolipoma in Kidney, Liver, and Lymph Node: Case Report/Review of the Literature. Jornal Brasileiro de Patologia e Medicina Laboratorial, 51, 173-177. https://doi.org/10.5935/1676-2444.20150030
[27]  Molina, T.I., Montes, J.M., Cecilia, E.C., Muñiz, M.D.M.M., González, A.G. and Martínez, M.A.H. (2009) Angiomyolipomas, Tuberous Sclerosis and Pregnancy. Ginecología y Obstetricia de México, 77, 380-386.
[28]  Schneider-Monteiro, E.D., Lucon, A.M., Figueiredo, A.A.D., Junior, A.J.R. and Arap, S. (2003) Bilateral Giant Renal Angiomyolipoma Associated with Hepatic Lipoma in a Patient with Tuberous Sclerosis. Revista do Hospital das Clínicas, 58, 103-108. https://doi.org/10.1590/S0041-87812003000200008
[29]  Silva, A.A.D., Carlos, R., Contreras, E., Almeida, O.P.D., Lopes, M.A. and Vargas, P.A. (2007) Angiomyolipoma of the Upper Lip: Case Report and Review of the Literature. Medicina Oral, Patologia Oral, Cirugia Bucal, 12, e101-104.
[30]  Bree, E.D., Stamatiou, D., Chryssou, E., Michelakis, D. and Tzardi, M. (2019) Late Local, Peritoneal and Systemic Recurrence of Renal Angiomyolipoma: A Case Report. Molecular and Clinical Oncology, 10, 43-48.
[31]  Fukuda, Y., Omiya, H., Takami, K., Mori, K., Kodama, Y., Mano, M., et al. (2016) Malignant Hepatic Epithelioid Angiomyolipoma with Recurrence in the Lung 7 years after Hepatectomy: A Case Report and Literature Review. Surgical Case Reports, 2, Article No. 31. https://doi.org/10.1186/s40792-016-0158-1
[32]  Wood, M.E., Vogel, V., Ng, A., Foxhall, L., Goodwin, P. and Travis, L.B. (2012) Second Malignant Neoplasms: Assessment and Strategies for Risk Reduction. Journal of Clinical Oncology, 30, 3734-3745. https://doi.org/10.1200/JCO.2012.41.8681
[33]  Liu, Z., Liu, C., Guo, W., Li, S. and Bai, O. (2015) Clinical Analysis of 152 Cases of Multiple Primary Malignant Tumors in 15, 398 Patients with Malignant Tumors. PLOS ONE, 10, e0125754. https://doi.org/10.1371/journal.pone.0125754
[34]  Warren, S. and Gates, O. (1932) Multiple Primary Malignant Tumors: A Survey of the Literature and Statistical Study. The American Journal of Cancer Research, 16, 1358-1414.
[35]  Testori, A., Cioffi, U., Simone, M.D., Bini, F., Vaghi, A., Lemos, A.A., et al. (2015) Multiple Primary Synchronous Malignant Tumors. BMC Research Notes, 8, Article No. 730. https://doi.org/10.1186/s13104-015-1724-5
[36]  Sakellakis, M., Peroukid, S., Iconomou, G., Boumpoucheropoulos, S. and Kalofonos, H. (2014) Multiple Primary Malignancies: Report of Two Cases. Chinese Journal of Cancer Research, 26, 215-218.
[37]  Le, D.T., Do, K.H., Do, T.A., Bui, H.T.T. and Nguyen, C.V. (2022) Combined Large-Cell Neuroendocrine and Squamous Cell Carcinoma of the Uterine Cervix with a Personal History of the Primary Breast Duct Carcinoma in Situ: A Clinicopathological Characteristic and Outcome. Case Reports in Oncology, 15, 770-775. https://doi.org/10.1159/000526337
[38]  Gaengler, S., Andrianou, X.D., Piciu, A., Charisiadis, P., Zira, C., Aristidou, K., et al. (2017) Iodine Status and Thyroid Nodules in Females: A Comparison of Cyprus and Romania. Public Health, 143, 37-43. https://doi.org/10.1016/j.puhe.2016.10.027
[39]  Hsu, C.H., Huang, C.L., Hsu, Y.H., Iqbal, U., Nguyen, P.A. and Jian, W.S. (2014) Co-Occurrence of Second Primary Malignancy in Patients with Thyroid Cancer. QJM, 107, 643-648. https://doi.org/10.1093/qjmed/hcu051
[40]  Gabora, K., Bălăcescu, O., Trifa, A., Morariu, A.M., Pop, B., Visan, S., et al. (2022) Thyroid Carcinoma Associated with Other Primary Neoplasms, a Single Center Study. Medicine and Pharmacy Reports, 95, 275-281. https://doi.org/10.15386/mpr-2346

Full-Text


comments powered by Disqus

Contact Us

service@oalib.com

QQ:3279437679

WhatsApp +8615387084133

WeChat 1538708413