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盆腹腔巨大囊实性肿物

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楼主 发表于 2012-02-15 21:34|举报|关注(6)
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(盆腔腹腔肿物)混合性子宫内膜间质-平滑肌肿瘤(低级别,低度恶性)。

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42 楼    发表于2012-03-23 22:40:21举报|引用
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本帖最后由 abin 于 2012-03-23 22:45:52 编辑

值得学习。反省:双相性肿瘤也可能是上皮样平滑肌肿瘤。我的鉴别诊断库又丰富了,哈哈。

谢谢楼主。

另外建议楼主改进免疫组化质控,要有对照。据说,陈国璋教授亲自负责他们的免疫组化质控。

再啰嗦几句:从会诊所开的免疫组化项目分析的鉴别诊断思路包括:肌源性分化、子宫内膜间质分化、性索分化、SFT、上皮性分化、神经内分泌分化、GIST,考虑的都是常见病,都是常规思路。

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华夏病理/粉蓝医疗

为基层医院病理科提供全面解决方案,

努力让人人享有便捷准确可靠的病理诊断服务。


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41 楼    发表于2012-03-18 21:12:23举报|引用
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谢谢了,感谢楼主,有始有终

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40 楼    发表于2012-03-18 21:04:22举报|引用
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这例给我们2个启示:1、病理诊断还是要结合部位从常见病、多发病开始考虑,要从典型中找不典型,从不典型中找典型。2、免疫组化应该为HE形态服务,当出现矛盾时,以HE形态为准。

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39 楼    发表于2012-03-18 19:47:01举报|引用
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感谢版主告知最后诊断,从中学习了很多!

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将生命本质里最真实的想法付诸实践的勇气

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38 楼    发表于2012-03-18 12:45:04举报|引用
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有始有终,不错。

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Suffered from papillary thyroid carcinoma, then major in Endocrine tumor.

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37 楼    发表于2012-03-18 09:42:59举报|引用
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本帖最后由 Renghis 于 2012-03-18 09:52:05 编辑

 

中山大学附属肿瘤医院 会诊结果:

混合性子宫内膜间质-平滑肌肿瘤(低级别,低度恶性)

 

本例纯粹被免疫组化坑了!

我院免疫组化SMA和CD10完全阴性,可在会诊医院却显示阳性,会诊医院加做HHF35也是阳性(SMA、CD10及HHF35阳性范围及强度不清楚)。由此认为,HE形态学还是放在第一位,当HE形态强烈怀疑某个肿瘤,而关键免疫组化不支持时,这时就要好好思索是不是免疫组化的问题了,可以加做对照或使用外院抗体。

 

 


名称:图1
描述:P1020687

 

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36 楼    发表于2012-03-05 08:39:49举报|引用
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很好的病例!学习中

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35 楼    发表于2012-03-05 07:54:03举报|引用
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引用 31 楼 pathologybz 在 2012-03-04 14:28:32 的发言:

楼主所说的阴性标记是丁点也不表达吗?那可难了!


一丁点儿也不表达!影像学及术中所见卵巢一丁点儿事都没有!肿物与卵巢没有关系!一有会诊结果,立即告知大家!

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34 楼    发表于2012-03-04 22:19:42举报|引用
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期待会诊结果!

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好好学习

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33 楼    发表于2012-03-04 15:13:13举报|引用
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本例从大体形态、组织学和免疫表型看,首先还是应该考虑卵巢纤维瘤、卵泡膜纤维瘤或富于细胞性纤维瘤,具体哪个要看组织切片决定。

理由如下:

1、大体上囊实性,这是卵巢纤维瘤或卵泡膜纤维瘤常见的表现。

2、组织学由一致的梭形细胞构成,间质有水肿、粘液样变,略呈结节状改变。据楼主的观察核分裂少见。

3、免疫组化表达desmin、CD56、Vimentin、CD99,这些与假设诊断并不矛盾。

Mod Pathol. 1998 Jul;11(7):656-64.

Inhibin expression in ovarian tumors and tumor-like lesions: an immunohistochemical study.

Source

Department of Pathology, University of Mainz, Germany.

Abstract

We investigated 203 ovarian tumors and tumor-like lesions for inhibin expression using a monoclonal anti-inhibin alpha antibody. Inhibin was present in the tumor cells in all 14 primary adult granulosa cell tumors (4 luteinized) plus 3 metastatic, all 10 primary juvenile granulosa cell tumors plus 1 metastatic, 10 of 11 thecomas, 3 of 11 fibromas, 4 of 11 sclerosing stromal tumors, 6 of 11 Sertoli cell tumors (1 oxyphilic), 7 of 11 Sertoli-Leydig cell tumors, 1 gynandroblastoma, 10 primary ovarian sex cord tumors with annular tubules plus 2 metastatic, 8 of 9 steroid cell tumors, both pregnancy luteomas, 1 of 2 unclassified sex cord tumors, 2 of 5 gonadoblastomas, 9 of 10 female adnexal tumors of probable wolffian origin, and in the non-neoplastic stroma of many carcinomas and germ cell tumors. The tumor cells were inhibin-negative in 10 fibrosarcomas, 12 small cell carcinomas of hypercalcemic type, 24 germ cell tumors (except for a focus of inhibin-positive syncytiotrophoblast in one case), and 17 ovarian carcinomas. Two of the three inhibin-positive fibromas showed diffuse immunostaining and were associated with evidence of estrogenic activity. Among nine Sertoli-Leydig cell tumors with available clinical data, four that were more than minimally inhibin-positive were accompanied by androgenic manifestations; five inhibin-negative or only minimally positive tumors lacked such evidence. Inhibin immunostaining may be useful in the differential diagnosis of inhibin-positive sex cord tumors versus histologically similar inhibin-negative neoplasms, but inhibin negativity does not preclude a diagnosis of sex cord tumor. The unexpected, common inhibin positivity of female adnexal tumors of probable wolffian origin indicates that inhibin staining cannot be used to differentiate these tumors from Sertoli cell tumors. Inhibin immunostaining is also helpful in identifying potential steroid hormone-secreting cells in the non-neoplastic stromal component of epithelial, germ cell, and other ovarian tumors.

 

Am J Surg Pathol. 2008 Jun;32(6):884-90.

Expression of CD56 and WT1 in ovarian stroma and ovarian stromal tumors.

Source

Division of Pathology, City of Hope National Medical Center, Los Angeles, CA, USA.

Abstract

The immunophenotype of ovarian stroma and spindle cell tumors derived from ovarian stroma has not been well studied. We studied the expression of CD56, WT1, estrogen receptor-beta (ER-beta), progesterone receptor (PR), smooth muscle actin, S-100, CD34, and muscle specific actin in 16 normal ovaries, 17 ovarian fibromas, 11 ovarian cellular fibromas, 10 ovarian fibrothecomas, and 11 ovarian leiomyomas. In addition, we studied CD56 and WT1 expression in 7 cases of normal endometrium, 8 uterine smooth muscle tumors, 5 endometrial stromal tumors and 64 nongynecologic (GYN) spindle cell sarcomas. All normal ovaries, ovarian fibromas, fibrothecomas, and ovarian leiomyomas were positive for CD56 and WT1. Most of the normal ovaries, ovarian fibromas, ovarian fibrothecomas, and ovarian leiomyomata also expressed ER-beta and PR. Eight of 17 ovarian fibromas, 5 of 11 ovarian cellular fibromas, and 4 of 10 ovarian fibrothecoma with focal fibroblastic differentiation were positive for smooth muscle actin. A few cases of these tumors also expressed S-100 and CD34. Only rare cases of non-GYN spindle cell sarcomas expressed WT1. Our study results show that ovarian fibromas, fibrothecomas, and leiomyomas have a similar immunophenotype (positive for CD56, WT1, ER-beta, and PR) to that of ovarian stromal cells, supporting an ovarian stromal origin for these neoplasms. However, unlike normal ovarian stromal cells, ovarian fibromas, fibrothecomas, and leiomyomas can also show fibroblastic, smooth muscle, Schwannian, and solitary fibrous tumorlike differentiation. WT1 is a fairly specific marker for spindle cell tumors of gynecologic organs, including ovarian spindle cell tumors, endometrial stromal tumors, and uterine smooth muscle tumors. Non-GYN spindle cell sarcomas rarely express WT1. CD56 is strongly expressed in ovarian stromal cells but not in endometrial stromal cells. CD56 is often expressed by a wide variety of spindle cell sarcomas, thus, it has no value in differentiating GYN from non-GYN spindle cell tumors.

Arch Pathol Lab Med. 1990 May;114(5):502-5.

Immunohistochemical analysis for desmin in normal and neoplastic ovarian stromal tissue.

Source

Department of Pathology, Columbia Presbyterian Medical Center, New York, NY 10032.

Abstract

Ovarian stroma contains cells with the ultrastructural features of smooth-muscle cells. The purpose of this study was to analyze normal ovaries, ovarian stromal tumors (fibroma/thecomata and granulosa cell tumors), and ovarian leiomyomata for desmin reactivity. Groups of ovarian stromal cells that expressed desmin were noted in six of six normal ovaries. Desmin was also detected in two of six fibroma/thecomata and two of two ovarian leiomyomata. The number of tumor cells with detectable desmin was much greater in the leiomyomata. Desmin was not detected in any of six granulosa cell tumors. We conclude that stromal cells with an immunohistochemical feature of smooth-muscle cells are routinely found in normal ovaries. This study demonstrates the usefulness of immunohistochemistry in corroborating the diagnosis of ovarian leiomyomata, although desmin positivity per se is not diagnostic of ovarian leiomyomata, and also raises the possibility that some ovarian leiomyomata may be derived from stromal cells.

 

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32 楼    发表于2012-03-04 14:46:58举报|引用
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本帖最后由 pathologybz 于 2012-03-04 14:47:27 编辑

还有个问题,本例中右侧卵巢有事吗?从手术描述看右侧卵巢好像没有事情啊。

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31 楼    发表于2012-03-04 14:28:32举报|引用
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楼主所说的阴性标记是丁点也不表达吗?那可难了!

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30 楼    发表于2012-03-04 12:41:57举报|引用
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引用 27 楼 xhyong 在 2012-03-03 20:29:47 的发言:

会诊结果?

 

会诊结果尚未回来,一有会诊结果,立即告知大家!!!必须的!!!

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29 楼    发表于2012-03-04 12:19:44举报|引用
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本例我感觉在于SFT和上皮样平滑肌(血管来源)瘤鉴别,但是SFT不会出现肌源性免疫组化的阳性表达,所以结合免疫组化,考虑为上皮样平滑肌瘤(血管平滑肌来源),因为仔细寻找,肿瘤细胞和血管平滑肌瘤细胞是有一定过度的。

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28 楼    发表于2012-03-04 12:12:19举报|引用
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版主,会诊结果出来了吗?

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27 楼    发表于2012-03-03 20:29:47举报|引用
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会诊结果?

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26 楼    发表于2012-02-24 19:28:00举报|引用
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该例患者家属已经拿出去会诊,一有会诊结果即告知大家!

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25 楼    发表于2012-02-24 11:14:24举报|引用
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SFT?平滑肌来源?

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24 楼    发表于2012-02-22 22:38:24举报|引用
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加做DOG1免疫组化。E-GIST 仍不能完全排除

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Chenjoan

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23 楼    发表于2012-02-22 11:53:22举报|引用
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引用 22 楼 何生 在 2012-02-22 10:34:33 的发言:

建议再多取材,是否可找到多一些成分。

之后在不同切面补取了6块,镜下图像都很相似。

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