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[一例卡尼综合征病例]

[A case of Carney complex].

作者信息

Scherer K, Müller T, Stolz W, Aebert H, Schunkert H

机构信息

Klinik und Poliklinik für Innere Medizin II, Klinikums der Universität Regensburg.

出版信息

Dtsch Med Wochenschr. 1998 Aug 14;123(33):972-6. doi: 10.1055/s-2007-1024106.

DOI:10.1055/s-2007-1024106
PMID:9739345
Abstract

HISTORY AND CLINICAL FINDINGS

For some months a 57-year-old woman had noted increasing shortness of breath, associated in the last few weeks with undirected vertigo and several brief periods of lost consciousness. She was finally admitted because of additional central facial paresis. On auscultation a high-frequency systolic murmur was heard over the apex and a discrete diastolic murmur over Erb's point. There were numerous facial freckles and three cutaneous myxomas.

INVESTIGATIONS

Echocardiography revealed irregular tumours throughout the left atrium and a large broad-based one prolapsing through the mitrale valve in diastole. Computed tomography demonstrated a 6 x 6 cm tumour in the left lower abdomen, probably arising from the left ovary, and a second 3 x 3 cm presacral tumour.

TREATMENT AND COURSE

At cardiac surgery four tumours were found in the left atrium and resected: histologically they were benign myxomas. Removal required extensive resection in the area of the interatrial septum and the atrial wall, resulting in 2 degrees AV block for which a VDD pacemaker was implanted.

CONCLUSION

Atrial myxomas may be the cardinal sign of the Carney Complex, an autosomal dominant syndrome with cutaneous myxomas, myxoid abdominal tumours, hormone-producing tumours in the testicles, adrenal cortex or hypophysis, schwannoma as well as lentigines. For this reason, further tumours should be looked for if freckles and/or cutaneous tumours are found in association with an atrial myxoma. The patient and family should be informed about the genetic aspects.

摘要

病史及临床检查结果

数月来,一名57岁女性出现气短加重,在过去几周内伴有不明原因的眩晕及数次短暂意识丧失。最终因出现额外的中枢性面瘫而入院。听诊时在心尖部闻及高频收缩期杂音,在Erb点闻及舒张期杂音。患者面部有大量雀斑及3处皮肤黏液瘤。

检查

超声心动图显示左心房内有多个不规则肿瘤,一个大的基底较宽的肿瘤在舒张期经二尖瓣脱垂。计算机断层扫描显示左下腹有一个6×6 cm的肿瘤,可能起源于左卵巢,还有一个3×3 cm的骶前肿瘤。

治疗及病程

心脏手术时在左心房发现4个肿瘤并切除:组织学检查为良性黏液瘤。切除肿瘤需要广泛切除房间隔及心房壁区域,导致二度房室传导阻滞,为此植入了VDD起搏器。

结论

心房黏液瘤可能是Carney综合征的主要体征,这是一种常染色体显性综合征,伴有皮肤黏液瘤、黏液样腹部肿瘤、睾丸、肾上腺皮质或垂体的激素分泌肿瘤、神经鞘瘤以及雀斑样痣。因此,如果发现雀斑和/或皮肤肿瘤与心房黏液瘤同时存在,应进一步寻找其他肿瘤。应告知患者及其家属相关遗传方面的情况。

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Familial atrial myxoma.家族性心房黏液瘤
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