骨髓发育不全:未经治疗的格雷夫斯病的罕见并发症。

Juliana Garcia, Larissa de França, Vivian Ellinger, Mônica Wolff
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引用次数: 9

摘要

甲亢的非典型表现形式对临床医生来说一直是一个挑战。我们报告一位女性患者,其典型症状为甲状腺毒症,既往未使用过硫胺类药物治疗,伴全血细胞减少症,达到甲状腺功能正常状态后恢复。虽然格雷夫斯病中全血细胞减少的主要病例被认为是抗甲状腺药物(硫胺)的并发症,但在本病例中,血液检查的改变与未经治疗的甲状腺功能亢进有关。在文献综述中,我们发现了1981年至2012年间的19例病例报告,但它与高细胞骨髓伴表皮破坏有关。然而,我们的病例是一个没有纤维化或脂肪组织替代的低细胞骨髓,在甲状腺治疗后,其外周血管得到改善。虽然罕见,全血细胞减少症,当存在时,可能发展为一个不寻常的和严重的表现,在未经治疗的受试者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Marrow hypoplasia: a rare complication of untreated Grave's disease.

Atypical presentation forms of hyperthyroidism are always a challenge to the clinician. We present a female patient with the typical symptoms of thyrotoxicosis, without any thionamides treatment before, associated with pancytopenia, which recovered after euthyroidism state was achieved. Although the major cases of pancytopenia in Grave's disease are seen as a complication of antithyroid drugs (thioamides), in this case report the alteration in blood tests was associated with untreated hyperthyroidism. In the literature review, we found 19 case reports between 1981 to 2012, but it has been related to a hypercellular bone marrow with periferic destruction. Our case, however, is about a hypocellular bone marrow without fibrosis or fat tissue replacement, which proceeded with a periferic improvement following thyroid treatment. Although rare, pancytopenia, when present, may develop as an unusual and severe manifestation in untreated subjects.

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