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  青岛大学学报(医学版)  2020, Vol. 56 Issue (1): 109-111   DOI: 10.11712/jms.2096-5532.2020.56.006
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基金项目

山东省自然科学基金项目(ZR2019MH121)

引用本文 [复制中英文]

刘婷婷, 王翔宇, 韩毅, 等. 子宫脂肪平滑肌瘤临床及病理学特征探讨(附1例报告及文献复习)[J]. 青岛大学学报(医学版), 2020, 56(1): 109-111.   DOI: 10.11712/jms.2096-5532.2020.56.006
[复制中文]
LIU Tingting, WANG Xiangyu, HAN Yi, et al. Clinical and pathological features of uterine lipoleiomyoma: a case report and literature review[J]. Journal of Qingdao University(Medical Sciences), 2020, 56(1): 109-111.   DOI: 10.11712/jms.2096-5532.2020.56.006
[复制英文]

作者简介

刘婷婷(1990-),女,硕士研究生.

通讯作者

崔竹梅(1966-),女,博士,主任医师,博士生导师。E-mail:cuizhumei1966@126.com.

文章历史

收稿日期:2019-06-06
修订日期:2019-10-21
子宫脂肪平滑肌瘤临床及病理学特征探讨(附1例报告及文献复习)
刘婷婷1 , 王翔宇1 , 韩毅1 , 闫伟华2 , 崔竹梅1     
1. 青岛大学附属医院妇科, 山东 青岛 266100;
2. 青岛大学附属医院病理科, 山东 青岛 266100
摘要目的 探讨子宫脂肪平滑肌瘤的临床及病理学特征。方法 对1例子宫脂肪平滑肌瘤病人的临床资料进行分析,并结合文献探讨子宫脂肪平滑肌瘤的临床及病理特征。结果 病人为23岁女性,常规查体发现子宫肌瘤,超声检查怀疑其脂肪变性。行腹腔镜下子宫肌瘤剔除术,术后病理诊断为子宫脂肪平滑肌瘤。子宫脂肪平滑肌瘤病人的临床表现与子宫平滑肌瘤相似。病理检查显示肿瘤由脂肪组织、平滑肌及少量纤维组织构成;免疫组化显示平滑肌肌动蛋白阳性,Ki-67阳性率<1%。结论 子宫脂肪平滑肌瘤是一种极为罕见的良性肿瘤,诊断应结合病史、病理形态学特征及免疫组织化学检查结果。
关键词子宫肿瘤    平滑肌瘤    病理学, 临床    
Clinical and pathological features of uterine lipoleiomyoma: a case report and literature review
LIU Tingting1 , WANG Xiangyu1 , HAN Yi1 , YAN Weihua2 , CUI Zhumei1     
Department of Gynaecology, The Affiliated Hospital of Qingdao University, Qingdao 266100, China
ABSTRACT: Objective To investigate the clinical and pathological features of uterine lipoleiomyoma. Methods The clinical data of one patient with uterine lipoleiomyoma were analyzed, and the clinical and pathological features of uterine lipoleiomyoma were analyzed based on a literature review. Results The 23-year-old female patient was found to have uterine myoma on physical examination, and ultrasound suspected fatty degeneration of uterine myoma. Laparoscopic myomectomy was performed, and the patient was diagnosed with uterine lipoleiomyoma based on postoperative pathology. Patients with uterine lipoleiomyoma had similar clinical manifestations to those with uterine leiomyoma. Pathological examination showed that the tumor was composed of adipose tissue, smooth muscle, and a small amount of fibrous tissue, and immunohistochemistry showed positive smooth muscle actin and a Ki-67 positive rate of < 1%. Conclusion Uterine lipoleiomyoma is an extremely rare benign tumor, and diagnosis should be given based on medical history, pathological and morphological features, and immunohistochemistry results.
KEY WORDS: uterine neoplasms    leiomyoma    pathology, clinical    

子宫脂肪平滑肌瘤是一种良性肿瘤,由平滑肌细胞和成熟脂肪细胞构成,术前极易误诊,目前文献报道病例极少,确切的发病机制尚不清楚。2019年4月,我科收治1例子宫脂肪平滑肌瘤病人,本文对其临床资料进行分析,并参考国内外相关文献,探讨子宫脂肪平滑肌瘤的临床及病理学特征,为该病诊断和治疗提供依据。

1 临床资料 1.1 一般资料

病人,女,23岁。因“发现子宫肌瘤变性20 d”入院。妇科查体:外阴发育正常;阴道内未见异常,宫颈重度糜烂;子宫后位,增大如50 d妊娠大小,质软,无压痛;双侧附件区未扪及明显异常。妇科超声检查:子宫后壁见略高回声结节,大小为3.9 cm×3.4 cm×2.9 cm,边界尚清,超声检查结果提示子宫肌瘤并脂肪变(图 1A)。病人在全身麻醉下行腹腔镜子宫肌瘤剔除术。术中所见:子宫后壁近宫底部外突肌瘤直径约4 cm,手术剥除肌瘤,肌瘤质软呈淡黄色。病人术前没有行MRI及CT检查。术中快速冷冻病理检查结果提示子宫平滑肌瘤。病人术后恢复良好。

A:子宫脂肪平滑肌瘤的超声表现;B:苏木精-伊红染色,400倍;C:免疫组化SMA阳性,400倍;D:免疫组化Ki-67阳性,100倍。 图 1 子宫脂肪平滑肌瘤的超声检查和病理观察
1.2 病理检查

肉眼观察:子宫肌瘤灰红组织多块,合计大小为5.5 cm×4.0 cm×1.0 cm,切面呈灰白色,质软。光镜检查:平滑肌细胞与脂肪细胞混合存在,主要成分为平滑肌细胞,脂肪细胞为单泡细胞,胞质成分位于细胞边缘,中央为大脂滴。免疫组化检查显示:平滑肌肌动蛋白(SMA)阳性,Ki-67阳性率<1%。见图 1B~D。病理诊断为子宫脂肪平滑肌瘤。

2 讨论

子宫脂肪平滑肌瘤非常罕见,相关文献报告其发病率为0.03%~0.25%[1-2],约占子宫平滑肌瘤的0.2%[3]。子宫脂肪平滑肌瘤通常发生在绝经后的妇女[4-5],极少病人为育龄期。本例病人23岁,为年轻育龄期女性,不同于既往文献报道的好发年龄。大多数子宫脂肪平滑肌瘤病人无明显临床症状,部分病人可自扪及腹部包块,若肿瘤贴近子宫内膜或突向宫腔可出现不规则阴道流血,可有其他合并肿瘤。超声和CT检查结果为非特异性。虽然术前MRI检查可确定病变的脂肪性质[6],但大多数病例为术后组织病理学检查而确诊。该病人超声检查提示子宫肌瘤并脂肪变可能性大,术后病理显示平滑肌细胞与脂肪细胞混合存在,主要成分为平滑肌细胞,脂肪细胞为单泡细胞,胞质成分位于细胞边缘,中央为大脂滴。结合免疫组化SMA阳性、Ki-67阳性率<1%,诊断为子宫脂肪平滑肌瘤。子宫脂肪平滑肌瘤可能同时存在于子宫、卵巢和输卵管恶性肿瘤中,也可能有其他代谢紊乱和雌激素异常。因参考资料较少,术前辅助检查误诊较多。子宫脂肪平滑肌瘤大多数为良性[7],有极少数病例报道有恶变。免疫组织化学检测在探讨其复杂的组织发生中有着不可缺少的作用[8-9]

妇科超声是目前妇科疾病检查首选方法[6, 10]。超声检查子宫脂肪平滑肌瘤表现为明确的高回声病变,与脂肪含量一致,可有低回声边缘[11]。与超声检查相比较,MRI及CT检查可明确病变中的脂肪成分以及肿瘤与周围器官的关系[12]。CT检查显示病变为脂肪衰减而不增强;MRI检查显示子宫脂肪平滑肌瘤T1、T2成像表现为高信号,DW成像表现为信号丢失[2, 13]。MRI检查还能确定肿瘤来源,分辨其与周围组织分界[2, 6, 10, 14]。若病理检查见脂肪细胞与平滑肌细胞共同存在,可明确诊断为子宫脂肪平滑肌瘤[15-16]

子宫脂肪平滑肌瘤多发生在宫体肌壁间,也可发生在宫颈[17-18],极少病例肿瘤位于阔韧带等特殊部位[19-20],可单发或多发[20]。肿瘤大小相差较多,结节状,一般界限明显,可有假包膜。肿瘤切面呈实性,灰黄色较多,肿瘤的色泽和质地与脂肪组织在肿瘤中所占的比例有关,若脂肪含量较少,则肿瘤切面呈灰粉色。病理检查可见脂肪细胞和平滑肌细胞共存[21],可同时伴有少量纤维组织;免疫组化结果提示SMA阳性,Ki-67阳性率<1%。大多数情况下细胞分化成熟,极少病例报道脂肪细胞有很大异形性(呈印戒状,有核仁,可见脂肪母细胞)[22],可考虑脂肪肉瘤。

子宫脂肪平滑肌瘤诊断时应与以下疾病鉴别:①子宫平滑肌瘤脂肪化生,病理检查见其一般伴有子宫平滑肌细胞变性及坏死[23-24];②平滑肌瘤脂肪变性,光镜下观察平滑肌细胞内可见脂滴,而非脂肪细胞[10];③脂肪肉瘤,发病率极低[2, 25],光镜下可见异形脂肪母细胞,核分裂象多见;④纤维脂肪瘤,由纤维组织和脂肪细胞构成,免疫组化可鉴别;⑤脂肪瘤,病例极少[10, 26-27],病理检查仅见脂肪细胞,无平滑肌细胞[28]

关于脂肪组织来源的假说众多,均尚未完全确定。目前研究有以下观点:①平滑肌组织或结缔组织脂肪化生[1, 22];②直接来源于间叶细胞;③来源于染色体异位后的变异,有研究显示5号染色体可能与脂肪平滑肌瘤的形成有关[9, 22];④与子宫平滑肌瘤发生机制相似[29]

综上所述,子宫脂肪平滑肌瘤是一种良性肿瘤,由平滑肌细胞和成熟脂肪细构成。子宫脂肪平滑肌瘤较为罕见,术前极易误诊,应结合病史、病理学特征及免疫组织化学检查结果进行诊断。

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