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Case Reports
. 2020 Jun 14;10(3):238-241.
doi: 10.1080/20009666.2020.1770019.

Pure red cell aplasia and seronegative myasthenia gravis in association with thymoma

Affiliations
Case Reports

Pure red cell aplasia and seronegative myasthenia gravis in association with thymoma

Sun Yong Lee et al. J Community Hosp Intern Med Perspect. .

Abstract

Pure red cell aplasia is an uncommon paraneoplastic syndrome of thymoma. Myasthenia gravis is the most common paraneoplastic syndrome associated with thymoma. We present a case of a 79-year-old Pacific Islander female who presented with profound fatigue, generalized weakness, significant unintentional weight loss, bilateral ptosis, and anemia. The bone marrow biopsy showed near absence of erythroid elements consistent with pure red cell aplasia. Ice-pack test was consistent with myasthenia gravis and computed tomography of the chest demonstrated a thymoma. The patient was started on immunosuppressive treatment with prednisone and cyclosporine. This case demonstrates a rare combination of paraneoplastic manifestations of thymoma: pure red cell aplasia and myasthenia gravis.

Keywords: Pure red cell aplasia; ice-pack test; myasthenia gravis; paraneoplastic syndrome; thymoma.

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Conflict of interest statement

No potential conflict of interest was reported by the authors.

Figures

Figure 1.
Figure 1.
Positive ice pack test. A marked improvement of ptosis is noted after ice pack application for 2 minutes.
Figure 2.
Figure 2.
Bone marrow biopsy slides, demonstrating near absence of erythroid elements. (a) Low-power view of a HE-stained section (x20). (b) High-power view of a HE-stained section (x400). (c) Low-power view of a CD71 stain for confirmation of pure red cell aplasia.
Figure 3.
Figure 3.
Computed tomography (CT) chest without contrast revealed ovoid anterior mediastinal mass consistent with thymoma. (a) Green arrow. (b) Diameter measurement of thymoma, 5.6 × 3.1 cm ovoid anterior mediastinal mass.

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