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Splenic Silicosis
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Eric Andrey Rodríguez-Vega
, Karen Pamela Martínez-Espinosa, Ana Linet Bravo-Gutiérrez
National Institute of Respiratory Diseases “Ismael Cosío Villegas”, Calzada de Tlalpan 4502, Tlalpan, Sección XVI, 14080 Ciudad de México, Mexico
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A 46-year-old man, who had worked as a sculptor for 30 years and had never smoked, was referred to the emergency department with a two-month history of productive cough, pleuritic chest pain, and progressive dyspnea. Physical examination revealed respiratory distress and digital clubbing. Laboratory tests—including complete blood count, renal function, and immunoglobulin levels—were within normal limits. High-resolution computed tomography (HRCT) of the chest revealed a right-sided pneumothorax, irregular bilateral hilar masses (Panels A and E, arrows), and mediastinal lymphadenopathy with eggshell calcifications (Panels B and E, arrows). Diffuse punctate calcifications were also observed in the spleen (Panels C and D, arrowheads). Tests for human immunodeficiency virus, histoplasma antigen, mycobacterial cultures, and GenXpert were negative. The clinical–radiological diagnosis of chronic silicosis with splenic involvement, a rare extrapulmonary manifestation, was established [1,2]. This presentation is associated with intense and prolonged exposure to silica [3,4]. The patient underwent right-sided chemical pleurodesis and started bronchodilator therapy. At follow-up, he remained clinically stable, required supplemental oxygen, and had no recurrence of pneumothorax (Fig. 1).

Fig. 1.

Chest CT scans in coronal and axial views. (Panel A) Right pneumothorax observed. (Panels B and E, arrows) show the presence of bilateral irregular calcified masses located in the hilar regions. (Panels B and F, arrows) Multiple “eggshell” calcifications of mediastinal lymph nodes. (Panels C–E arrowheads) Diffuse microcalcifications in the spleen.

Author's contributions

All authors have participated equally in the preparation, writing and revision of the manuscript.

Informed consent

Informed consent has been obtained from the patient.

Funding

The present research has not received specific grants from public sector agencies, commercial sector or non-profit entities.

Conflicts of interest

The authors state that they have no conflict of interests.

References
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T.C. Shen, C.H. Chen.
Silicosis with splenic involvement.
QJM, 106 (2013), pp. 89-90
[2]
M. Bai, D.P. Dwivedi, V.M. Babu, L.S. Warrier, A.S. Chauhan.
Splenic silicosis: a rare cause of splenic calcifications.
Indian J Occup Environ Med, 25 (2021), pp. 185-187
[3]
M.C. Carreño Hernández, S. Garrido Paniagua, M. Colomés Iess, et al.
Accelerated silicosis with bone marrow, hepatic and splenic involvement in a patient with lung transplantation.
[4]
N. Consul, S. Javed-Tayyab, C. Lall, C.T. Jensen, C.O. Menias, P.J. Pickhardt, et al.
Calcified splenic lesions: pattern recognition approach on CT with pathologic correlation.
Am J Roentgenol, 214 (2020), pp. 1083-1091
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