Renal oncocytoma in a female patient with rheumatoid arthritis and secondary Sjögren’s syndrome: Non-coincidental link to autoimmunity?*

Авторы

  • Леонид Чурилов St. Petersburg State University, 7–9, Universitetskaya nab., St. Petersburg, 199034, Russian Federation
  • Жозелио Фрейре де Карвалью Institute for Health Sciences, Federal University of Bahia, Rua Augusto Viana, Palácio da Reitoria, Canela, Salvador, 40110–909, Brazil

DOI:

https://doi.org/10.21638/spbu11.2021.201

Аннотация

The objective of the article was to describe a female patient with rheumatoid arthritis (RA) and secondary Sjögren’s syndrome (SS) who developed a renal oncocytoma and was cured by percutaneous cryoablation therapy. A 72-year-old female patient with a long-term history of polyarthritis involving her hands, shoulders, knees, and ankles associated with morning stiffness and rheumatoid factor of 107 U/mL (nr: <29 U/mL) and anti-CCP of 121 U/mL (nr:<5 U/mL). A diagnosis of RA was determined 10 years ago, and prednisone with methotrexate were initiated, later changed for leflunomide 20mg/day. In 2014 a diagnosis of secondary SS was determined. In April 2014, during a routine abdominal ultrasound, a tumor was found in her left kidney. A magnetic resonance imaging confirmed a solid nodule with hypervascularization on the left kidney. She was submitted to a percutaneous cryoablation procedure without any intercurrence, and it had success. The histopathological analysis demonstrated a renal oncocytoma limited to the left kidney. No chemotherapy or radiotherapy was needed. After surgery, a flare of RA was noted and was resistant to methotrexate and sulfasalazine. Rituximab was then started, and she had an excellent progressive response. Minor thyroid changes were registered by ultrasound monitoring and signs of hyperparathyroidism manifested. This observation illustrates the first ever described case of a patient with RA and secondary SS who developed several years after the RA onset, a renal oncocytoma, and was successfully treated with cryoablation therapy. The possible links between oncocytic cell metaplasia/neoplasia and autoimmunity are discussed.

Ключевые слова:

Rheumatoid arthritis, Oncocytoma, Tumor, Neoplasia, Metaplasia, Dysplasia, Autoimmunity, Cancer, Immunosuppressive drugs, Sjögren’s syndrome, Hürthle-Askanazy cells, Hashimoto’s thyroiditis

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References

Scott D. L., Wolfe F., Huizinga T. W. Rheumatoid arthritis. Lancet, 2010, vol. 376, no. 9746, pp. 1094–1108.

De Cock D., Hyrich K. Malignancy and rheumatoid arthritis: Epidemiology, risk factors and management.Best Pract. Res. Clin. Rheumatol., 2018, vol. 32, no. 6, pp. 869–886.

Simon T. A., Thompson A., Gandhi K. K., Hochberg M. C., Suissa S. Incidence of malignancy in adult patients with rheumatoid arthritis: a meta-analysis [published correction appears in Arthritis Res Ther. 2016, vol. 18, no. 1, p. 100]. Arthritis. Res. Ther., 2015, vol. 17, no. 1, p. 212.

Gridley G., McLaughlin J. K., Ekbom A., Klareskog L., Adami H.-O., Hacker D. G., Hoover R., Fraumeni J. F. Jr. Incidence of cancer among patients with rheumatoid arthritis. J. Natl. Cancer Inst., 1993, vol. 85, no. 4, pp. 307–311. https://doi.org/10.1093/jnci/85.4.307

Kauppi M., Pukkala E., Isomäki H. Low incidence of colorectal cancer in patients with rheumatoid arthritis. Clin. Exp. Rheumatol., 1996, vol. 14, no. 5, pp. 551–553.

Miyamoto T., Okuda Y., Oyama T., Oyama H., Takasugi K. Incidence of cancer among Japanese patients with rheumatoid arthritis. Ryumachi., 1996, vol. 36, no. 5, pp. 741–745.

Abásolo L., Júdez E., Descalzo M. A., González-Alvaro I., Jover J. A., Carmona L., EMECAR Study Group. Cancer in rheumatoid arthritis: Occurrence, mortality, and associated factors in a South European population. Semin. Arthritis Rheum., 2008, vol. 37, no. 6, pp. 388–397. https://doi.org/10.1016/j.semarthrit.2007.08.006

Love T., Solomon D. H. The relationship between cancer and rheumatoid arthritis: still a large research agenda. Arthritis Res. Ther., 2008, vol. 10, no. 3, p. 109.

Wang J. L., Yin W. J., Zhou L. Y., Zhou G., Liu K., Hu C., Zuo X.-C., Wang Ya-F. Risk of non-melanoma skin cancer for rheumatoid arthritis patients receiving TNF antagonist: a systematic review and metaanalysis.Clin. Rheumatol., 2020, vol. 39, no. 3, pp. 769–778.

Fragoulis G. E., Chatzidionysiou K. Lung cancer in rheumatoid arthritis. Is there a need for better risk assessment and screening? Clin. Rheumatol., 2020, vol. 39, no. 3, pp. 957–961.

Liang Y., Yang Z., Qin B., Zhong R. Primary Sjogren’s syndrome and malignancy risk: a systematic review and meta-analysis. Ann. Rheum. Dis., 2014, vol. 73, no. 6, pp. 1151–1156.

Wobker S. E., Williamson S. R. Modern Pathologic Diagnosis of Renal Oncocytoma. J. Kidney Cancer VHL, 2017, vol. 4, no. 4, pp. 1–12.

Mete O., Asa S. L. Oncocytes, oxyphils, Hürthle, and Askanazy cells: Morphological and molecular features of oncocytic thyroid nodules. Endocr. Pathol., 2010, vol. 21, no. 1, pp. 16–24. https://doi.org/10.1002/path.4166.10.1007/s12022-009-9102-2

Canberk S., Lima A.-R., Correia M., Batista R., Soares P., Máximo V., Simões M. S. Oncocytic thyroid neoplasms: from histology to molecular biology. Diagn. Histopathol., 2019, vol. 25, no. 5, pp. 154–165.

Müller-Höcker J. Die onkozytäre Metaplasie/Neoplasie — Morphologie, Biochemie, Molekulargenetik. Pathologie, 1998, vol. 19, no. 2, pp. 104–114. https://doi.org/10.1002/path.4166.10.1007/s002920050261

Hürthle K. Beiträge zur Kenntniss des Secretionsvorgangs in der Schilddrüse. Archiv für die Gesamte Physiologie des Menschen und der Tiere, 1894, vol. 56, pp. 1–4.

Askanazy M. Pathologisch-anatomische Beiträge zur Kenntnis des Morbus Basedowii, insbesondere über die dabei auftretende Muskelerkrankung. Dtsch. Arch. f. Klin Med. (Leipzig), 1898, vol. 61,pp. 118–186.

Stuart A. The changing scene in Hashimoto’s disease: a review. Med. Hypotheses, 2011, vol. 77, no. 3,pp. 424–426. https://doi.org/10.1002/path.4166.10.1016/j.mehy.2011.05.035

Caturegli P., De Remigis A., Rose N. R. Hashimoto thyroiditis: clinical and diagnostic criteria. Autoimmun. Rev., 2014, vol. 13, no. 4–5, pp. 391–397. https://doi.org/10.1002/path.4166.10.1016/j.autrev. 2014.01.007

Montone K. T., Baloch Z. W., LiVolsi V. A. The thyroid Hürthle (oncocytic) cell and its associated pathologic conditions: a surgical pathology and cytopathology review. Arch. Pathol. Lab. Med., 2008,vol. 132, no. 8, pp. 1241–1250. https://doi.org/10.5858/2008-132-1241-TTHOCA

Masini-Repiso A. M., Bonaterra M., Spitale L., Di Fulvio M., Bonino M. I., Coleoni A. H., Orgnero-Gaisán E. Ultrastructural localization of thyroid peroxidase, hydrogen peroxide-generating sites, and monoamine oxidase in benign and malignant thyroid diseases. Hum. Pathol., 2004, vol. 35, no. 4, pp. 436–446. https://doi.org/10.1002/path.4166.10.1016/j.humpath.2003.03.001

Zimmermann F. A., Neureiter D., Feichtinger R. G., Trost A., Sperl W., Kofler B., Mayr J. A. Deficiency of respiratory chain complex I in Hashimoto thyroiditis. Mitochondrion.,2016, vol. 26, pp. 1–6. https://doi.org/10.1002/path.4166.10.1016/j.mito.2015.11.002

Dhillon A. P., Rode J., Leathem A., Papadaki L. Somatostatin: a paracrine contribution to hypothyroidism in Hashimoto’s thyroiditis. J. Clin. Pathol., 1982, vol. 35, no. 7, pp. 764–770. https://doi.org/10.1002/path.4166.10.1136/jcp.35.7.764

Churilov L. P., Sobolevskaia P. A., Stroev Y. I. Thyroid gland and brain: Enigma of Hashimoto’s encephalopathy.Best Pract. Res. Clin. Endocrinol. Metab., 2019, vol. 33, no. 6, 101364. https://doi.org/10.1016/j.beem.2019.101364

Marino Gammazza A., Rizzo M., Citarrella R., Rappa F., Campanella C., Bucchieri F., Patti A., Nikolic D., Cabibi D., Amico G., Conaldi P. G., San Biagio P. L., Montalto G., Farina F., Zummo G., de Macario E. C., Macario A. J. L., Cappello F. Elevated blood Hsp60, its structural similarities and cross-reactivity with thyroid molecules, and its presence on the plasma membrane of oncocytes point to the chaperonin as an immunopathogenic factor in Hashimoto’s thyroiditis. Cell Stress Chaperones, 2014, vol. 19, no. 3, pp. 343–353. https://doi.org/10.1002/path.4166.10.1007/s12192-013-0460-9

Kimura H. J., Chen C. Y., Tzou S. C., Rocchi R., Landek-Salgado M. A., Suzuki K., Kimura M., Rose N. R., Caturegli P. Immunoproteasome overexpression underlies the pathogenesis of thyroid oncocytes and primary hypothyroidism: Studies in humans and mice. PLoS One. 2009, vol. 4, no. 11, e7857.https://doi.org/10.1002/path.4166.10.1371/journal.pone.0007857

Forland M., Bannayan G. A. Minimal-change lesion nephrotic syndrome with renal oncocytoma. Am. J. Med., 1983, vol. 75, no. 4, pp. 715–720. https://doi.org/10.1002/path.4166.10.1016/0002-9343(83)90463-1

Stojanović N., Ignjatovic I., Kostov M., Mijović Z., Zivković S., Kosević B. Giant renal oncocytoma. Vojnosanit Pregl., 2013, vol. 70, no. 1, pp. 68–71. https://doi.org/10.1002/path.4166.10.2298/vsp1301068

Paul A., Villepelet A., Lefèvre M., Périé S. Oncocytic parathyroid adenoma. Eur. Ann. Otorhinolaryngol. Head Neck Dis., 2015, vol. 132, no. 5, pp. 301–303. https://doi.org/10.1002/path.4166.10.1016/j.anorl.2015.08.033

Haglund F., Hallström B. M., Nilsson I. L., Höög A., Juhlin C. C., Larsson C. Inflammatory infiltrates in parathyroid tumors. Eur. J. Endocrinol., 2017, vol. 177, no. 6, pp. 445–453. https://doi.org/10.1002/path.4166.10.1530/EJE-17-0277

Das D. K. Hürthle cell metaplasia in chronic lymphocytic thyroiditis: Role of age factor and review of literature on its molecular pathogenesis. Diagn. Cytopathol., 2019, vol. 47, no. 5, pp. 475–481. https://doi.org/10.1002/path.4166.10.1002/dc.24140

Cheng J. L., Beebe J. D., Nepple K. G., Zakharia Yo., Mullins R. F., Flamme-Wiese M. J., Thurtell renal oncocytoma. Am. J. Ophthalmol. Case Rep., 2018, vol. 12, pp. 55–60. https://doi.org/10.1002/path.4166.10.1016/j.ajoc.2018.09.005

Carmichael K. A. Hürthle cell carcinoma in a patient with Graves’ Disease. Mo Med., 2009, vol. 106,no. 5, pp. 366–368.

Rub R., Avidor Y., Messer G., Schreiber L. Bullous pemphigoid as an initial presentation of renal oncocytoma.Dermatology, 1999, vol. 198, no. 3, pp. 322–323.

Handra-Luca A., Bacci F. Multiple sclerosis and oncocytic thyroid carcinoma: fortuitous or drug-related association? Neurol. Sci., 2019, vol. 40, no. 4, pp. 883–885. https://doi.org/10.1007/s10072-018–3640–7

Hansson S. F., Korsgren S., Pontén F., Korsgren O. Enteroviruses and the pathogenesis of type 1 diabetes revisited: cross-reactivity of enterovirus capsid protein (VP1) antibodies with human mitochondrial proteins. J. Pathol., 2013, vol. 229, no. 5, pp. 719–728. https://doi.org/10.1002/path.4166

Zargar H., Samarasekera D., Khalifeh A., Remer E. M., O’Malley Ch., Akca O., Autorino R., Kaouk J. H. Laparoscopic vs percutaneous cryoablation for the small renal mass: 15-year experience at a single center. Urology, 2015, vol. 85, no. 4, pp. 850–855.

Okawa H., Gobara H., Matsui Y., Iguchi T., Hiraki T., Kanazawa S. Ureteral obstruction by sloughed tumor complicating cryoablation of a renal oncocytoma. Radiol. Case Rep., 2018, vol. 13, no. 6,pp. 1195–1198.

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Опубликован

16.06.2021

Как цитировать

Чурилов, Л., & Фрейре де Карвалью, Ж. (2021). Renal oncocytoma in a female patient with rheumatoid arthritis and secondary Sjögren’s syndrome: Non-coincidental link to autoimmunity?*. Вестник Санкт-Петербургского университета. Медицина, 16(2), 77–84. https://doi.org/10.21638/spbu11.2021.201

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