Autopsy and Case Reports
https://www.autopsyandcasereports.org/article/doi/10.4322/acr.2018.002
Autopsy and Case Reports
Article / Clinical Case Report

Occurrence of mesothelial/monocytic incidental cardiac excrescences in material from open-heart procedures: case reports and literature review

Vitor Gabriel Ribeiro Grossi; Karen Lee; Léa Maria Demarchi; Jussara Bianchi Castelli; Vera Demarchi Aiello

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Abstract

Mesothelial/monocytic incidental cardiac excrescences (MICE) are unusual findings during the histological analysis of material from the pericardium, mediastinum, or other tissues collected in open-heart surgery. Despite their somewhat worrisome histological appearance, they show a benign clinical course, and further treatment is virtually never necessary. Hence, the importance of recognizing the entity relays in its differential diagnosis, as an unaware medical pathologist may misinterpret it for a malignant neoplasm. Other mesothelial and histiocytic proliferative lesions, sharing very close histological morphology and immunohistochemistry features with MICE, have been described in sites other than the heart or the mediastinum. This similarity has led to the proposal of the common denomination “histiocytosis with raisinoid nuclei.” We report three cases from the pathology archives of the Heart Institute of São Paulo University (Incor/HC-FMUSP), diagnosed as “mesothelial/monocytic incidental cardiac excrescence,” with immunohistochemical documentation, and provide a literature review of this entity.

Keywords

Heart Diseases; Incidental Findings; Epithelium; Histiocytes

References

Amonkar G, Nagle K. Mesothelial/monocytic incidental cardiac excrescences of the heart: a report of three cases. Cardiovasc Pathol. 2015;24(6):399-400. [PMID:26251080] [https://doi.org/10.1016/j.carpath.2015.07.002].

Rosai J, Gold J, Landy R. The histiocytoid hemangiomas. A unifying concept embracing several previously described entities of skin, soft tissue, large vessels, bone and heart. Hum Pathol. 1979;10(6):707-30. [PMID:527967] [https://doi.org/10.1016/S0046-8177(79)80114-8].

Veinot JP, Tazelaar HD, Edwards WD, Colby TV. Mesothelial/monocytic incidental cardiac excrescences: cardiac MICE. Mod Pathol. 1994;7(1):9-16. [PMID:8159657]

Burke AB, Virmani R. Tumors of the heart and great vessels. Washington: Armed Forces Institute of Pathology; 1995. Atlas of Tumor Pathology Third Series.

Bando Y, Kitagawa T, Uehara H, et al. So-called mesothelial/monocytic incidental cardiac excrescences obtained during valve replacement surgery: report of three cases and literature review. Virchows Arch. 2000;437(3):331-5. [PMID:11037355] [https://doi.org/10.1007/s004280000232].

Courtice RW, Stinson W, Walley V. Tissue fragments recovered at cardiac surgery masquerading as tumoral proliferations. Evidence suggesting iatrogenic or artefactual origin and common occurrence. Am J Surg Pathol. 1994;18(2):167-74. [PMID:8291655] [https://doi.org/10.1097/00000478-199402000-00006].

Censi S, Dell’Amore A, Conti R, Lorenzini P. Cardiac mesothelialymonocytic-incidental-excrescence: more than an artifactual lesion? Interact Cardiovasc Thorac Surg. 2008;7(6):1201-3. [PMID:18782786] [https://doi.org/10.1510/icvts.2008.184499].

Argani P, Sternberg SS, Burt M, Adsay NV, Klimstra DS. Metastatic adenocarcinoma involving a mesothelial/monocytic incidental cardiac excrescence (cardiac MICE). Am J Surg Pathol. 1997;21(8):970-4. [PMID:9255262] [https://doi.org/10.1097/00000478-199708000-00013].

Ton O, Polat N, Mansuroglu D, Kabukcuoglu F. Mesothelial/monocytic incidental cardiac excrescence in a patient with antiphospholipid syndrome. Interact Cardiovasc Thorac Surg. 2011;13(6):657-9. [PMID:21908884] [https://doi.org/10.1510/icvts.2011.277921].

Miller DV, Revelo MP. Diagnostic pathology: cardiovascular. 2nd ed. Salt Lake City: Elsevier Amirsys, 2017.

Jiao N, Zhang W, Wang W, et al. Mesothelial/monocytic incidental cardiac excrescence: a case report and review of literature. Int J Clin Exp Pathol. 2014;7(9):6219-24. [PMID:25337273]

Michal M, Kazakov DV, Dundr P, et al. Histiocytosis with raisinoid nuclei: a unifying concept for lesions reported under different names as nodular mesothelial/histiocytic hyperplasia, mesothelial/monocytic incidental cardiac excrescences, intralymphatic histiocytosis, and others: a report of 50 cases. Am J Surg Pathol. 2016;40(11):1507-16. [PMID:27340746] [https://doi.org/10.1097/PAS.0000000000000687].

Michal M, Michal M. The unifying concept of histiocytosis with raisinoid nuclei: a new evidence that intravascular/intralymphatic histiocytosis and MICE belong in the same spectrum of lesions. Pathol Res Pract. 2017;213(3):292. [PMID:28214197] [https://doi.org/10.1016/j.prp.2016.12.024].

Askin FB, McCann BG, Kuhn C. Reactive eosinophilic pleuritis: a lesion to be distinguished from pulmonary eosinophilic granuloma. Arch Pathol Lab Med. 1977;101(4):187-91. [PMID:576785]

Kireeva SG. Reactive eosinophilic pleuritis. Arkh Patol. 1995;57(3):54-7. [PMID:7677583]

McDonnell TJ, Crouch EC, Gonzalez JG. Reactive eosinophilic pleuritis. A sequela of pneumothorax in pulmonary eosinophilic granuloma. Am J Clin Pathol. 1989;91(1):107-11. [PMID:2642637] [https://doi.org/10.1093/ajcp/91.1.107].

Halícek F, Rosai J. Histioeosinophilic granulomas in the thymuses of 29 myasthenic patients: a complication of pneumomediastinum. Hum Pathol. 1984;15(12):1137-44. [PMID:6389315] [https://doi.org/10.1016/S0046-8177(84)80308-1].

Michal M, Havlíček F. Immunohistochemical phenotypes of histioeosinophilic granulomas of thymus and reactive eosinophilic pleuritis. Acta Histochem. 1993;94(1):97-101. [PMID:8351972] [https://doi.org/10.1016/S0065-1281(11)80345-4].

Gómez-Sánchez ME, Azaña-Defez JM, Martínez-Martínez ML, López-Villaescusa MT. Intralymphatic histiocytosis: a report of 2 cases. Actas Dermosifiliogr. 2017;S0001-7310(17):30053-54.

Haitz KA, Chapman MS, Seidel GD. Intralymphatic histiocytosis associated with an orthopedic metal implant. Cutis. 2016;97(4):12-4. [PMID:27163920]

Tran TA, Tran Q, Carlson JA. Intralymphatic histiocytosis of the appendix and fallopian tube associated with primary peritoneal high-grade, poorly differentiated adenocarcinoma of Müllerian origin. Int J Surg Pathol. 2017;25(4):357-64. [PMID:28112040] [https://doi.org/10.1177/1066896916688307].


Publication date:
02/16/2018

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