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同时发生卵巢肿物,子宫内膜肿物,宫颈原位癌。

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楼主 发表于 2010-01-16 15:35|举报|关注(0)
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姓    名: ××× 性别:  女 年龄:  72岁
标本名称:  
简要病史:  
肉眼检查:  一侧附件切除标本,卵巢为一卵圆形结节状肿物所替代,大小7×4.5×3.5厘米,表面光滑,切面灰黄色,分叶状,质中。一侧附输卵管,长5.5厘米,直径0.5厘米,伞端开放,表面可见多个小囊肿,灰白色,壁薄,直径0.2-0.4厘米。
2、子宫及一侧附件切除标本,子宫大小9×7.5×4.5厘米,宫颈长3.5厘米,外口直径3厘米,可见一息肉,直径0.8厘米,外口粗糙,充血,子宫肌壁厚2.6厘米,未见肌瘤,内膜厚0.2厘米,子宫腔体、底部内膜可见广基底息肉状肿物,4×3×0.8厘米,切面灰白色,质中,未累及肌层。输卵管长6厘米,直径0.5厘米,表面颗粒状,伞端开放,卵巢大小3×1.5×0.8厘米,表面光滑,切面灰白色,质硬,宫颈一侧见一囊肿,直径0.7厘米,内壁光滑。
(宫颈病变未上传。)
  • 同时发生卵巢肿物,子宫内膜肿物,宫颈原位癌。图1
    图1
  • 同时发生卵巢肿物,子宫内膜肿物,宫颈原位癌。图2
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  • 同时发生卵巢肿物,子宫内膜肿物,宫颈原位癌。图3
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  • 同时发生卵巢肿物,子宫内膜肿物,宫颈原位癌。图4
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    图7
  • 同时发生卵巢肿物,子宫内膜肿物,宫颈原位癌。图8
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  • 同时发生卵巢肿物,子宫内膜肿物,宫颈原位癌。图9
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  • 同时发生卵巢肿物,子宫内膜肿物,宫颈原位癌。图10
    图10
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  • 同时发生卵巢肿物,子宫内膜肿物,宫颈原位癌。图12
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  • 同时发生卵巢肿物,子宫内膜肿物,宫颈原位癌。图13
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  • 同时发生卵巢肿物,子宫内膜肿物,宫颈原位癌。图14
    图14
  • 同时发生卵巢肿物,子宫内膜肿物,宫颈原位癌。图15
    图15
  • 同时发生卵巢肿物,子宫内膜肿物,宫颈原位癌。图16
    图16
  • 同时发生卵巢肿物,子宫内膜肿物,宫颈原位癌。图17
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  • 同时发生卵巢肿物,子宫内膜肿物,宫颈原位癌。图18
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  • 同时发生卵巢肿物,子宫内膜肿物,宫颈原位癌。图19
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  • 同时发生卵巢肿物,子宫内膜肿物,宫颈原位癌。图20
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  • 同时发生卵巢肿物,子宫内膜肿物,宫颈原位癌。图21
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  • 同时发生卵巢肿物,子宫内膜肿物,宫颈原位癌。图22
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  • 同时发生卵巢肿物,子宫内膜肿物,宫颈原位癌。图23
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  • 同时发生卵巢肿物,子宫内膜肿物,宫颈原位癌。图24
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  • 同时发生卵巢肿物,子宫内膜肿物,宫颈原位癌。图25
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  • 同时发生卵巢肿物,子宫内膜肿物,宫颈原位癌。图26
    图26
  • 同时发生卵巢肿物,子宫内膜肿物,宫颈原位癌。图27
    图27
  • 同时发生卵巢肿物,子宫内膜肿物,宫颈原位癌。图28
    图28
  • 同时发生卵巢肿物,子宫内膜肿物,宫颈原位癌。图29
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  • 同时发生卵巢肿物,子宫内膜肿物,宫颈原位癌。图30
    图30
  • 同时发生卵巢肿物,子宫内膜肿物,宫颈原位癌。图31
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  • 同时发生卵巢肿物,子宫内膜肿物,宫颈原位癌。图32
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  • 同时发生卵巢肿物,子宫内膜肿物,宫颈原位癌。图33
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  • 同时发生卵巢肿物,子宫内膜肿物,宫颈原位癌。图34
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  • 同时发生卵巢肿物,子宫内膜肿物,宫颈原位癌。图35
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  • 同时发生卵巢肿物,子宫内膜肿物,宫颈原位癌。图36
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  • 同时发生卵巢肿物,子宫内膜肿物,宫颈原位癌。图37
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  • 同时发生卵巢肿物,子宫内膜肿物,宫颈原位癌。图38
    图38
  • 同时发生卵巢肿物,子宫内膜肿物,宫颈原位癌。图39
    图39
  • 同时发生卵巢肿物,子宫内膜肿物,宫颈原位癌。图40
    图40
  • 同时发生卵巢肿物,子宫内膜肿物,宫颈原位癌。图41
    图41
  • 同时发生卵巢肿物,子宫内膜肿物,宫颈原位癌。图42
    图42
  • 同时发生卵巢肿物,子宫内膜肿物,宫颈原位癌。图43
    图43
  • 同时发生卵巢肿物,子宫内膜肿物,宫颈原位癌。图44
    图44
  • 同时发生卵巢肿物,子宫内膜肿物,宫颈原位癌。图45
    图45
  • 同时发生卵巢肿物,子宫内膜肿物,宫颈原位癌。图46
    图46
  • 同时发生卵巢肿物,子宫内膜肿物,宫颈原位癌。图47
    图47
  • 同时发生卵巢肿物,子宫内膜肿物,宫颈原位癌。图48
    图48
  • 同时发生卵巢肿物,子宫内膜肿物,宫颈原位癌。图49
    图49
  • 同时发生卵巢肿物,子宫内膜肿物,宫颈原位癌。图50
    图50
  • 同时发生卵巢肿物,子宫内膜肿物,宫颈原位癌。图51
    图51
  • 同时发生卵巢肿物,子宫内膜肿物,宫颈原位癌。图52
    图52
  • 同时发生卵巢肿物,子宫内膜肿物,宫颈原位癌。图53
    图53
  • 同时发生卵巢肿物,子宫内膜肿物,宫颈原位癌。图54
    图54
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本帖最后由 于 2010-01-16 15:40:00 编辑
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1 楼    发表于2010-01-17 15:07:00举报|引用
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 马老师已经做了精辟的分析和点评。本例倾向富于细胞性纤维瘤或纤维瘤/卵泡膜瘤。肿瘤没有出血坏死。核分裂似乎也不是很多。不考虑恶性(只有当>3个核分裂/10个HPF时才有可能考虑)。鉴别诊断肉瘤样颗粒细胞瘤,好像也不够。

子宫的肿块被考虑为宫内膜息肉,伴有局部复杂性增生。不典型增生不能确定,毕竟图片显示的信息有限。

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2 楼    发表于2010-01-20 03:08:00举报|引用
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本帖最后由 于 2010-01-20 03:10:00 编辑

(1)  卵巢:纤维瘤/卵泡膜瘤 fibrothecoma, 细胞的密度比较大,可以叫 cellular fibrothecoma。如果分裂相>=4个核分裂/10个HPF-->就叫mitotically active cellular fibrothecoma。

Am J Surg Pathol. 2006 Aug;30(8):929-38.

Cellular fibromas of the ovary: a study of 75 cases including 40 mitotically active tumors emphasizing their distinction from fibrosarcoma.

Irving JA, Alkushi A, Young RH, Clement PB.

Department of Pathology, Vancouver General Hospital and the University of British Columbia, Vancouver, BC, Canada. Julie.Irving@vch.ca

Cellular fibroblastic tumors of the ovary are currently classified as either cellular fibroma (CF) or fibrosarcoma. The former are characterized by bland nuclei, 3 or fewer mitotic figures per 10 high-power fields (MFs/10 HPFs), and a low malignant potential, whereas fibrosarcomas usually have severe nuclear atypia, > or = 4 MFs/10 HPFs, and an aggressive clinical course. The prognosis of cellular fibromatous tumors with > or = 4 MFs/10 HPFs and low-grade cytology is not established and it is the purpose of this study to investigate that aspect. It has been our anecdotal experience that otherwise typical CFs with > or = 4 MFs/10 HPFs usually have a benign clinical course, suggesting that such tumors should be regarded as "mitotically active cellular fibroma" (MACF) rather than fibrosarcoma. Seventy-five cellular fibromatous neoplasms were analyzed to determine their clinicopathologic features and the appropriateness of "MACF" as a designation for otherwise typical CFs with > or = 4 MFs/10 HPFs. The mean age of patients with CF (n = 35, 0 to 3 MFs/10 HPFs) and MACF (n = 40, > or = 4 MFs/10 HPFs) was 51 and 41 years, respectively. Patients most commonly presented with symptoms related to a pelvic mass. All tumors were unilateral. The mean tumor size of CFs was 8.0 cm and 9.4 cm for MACFs. The majority of the tumors were solid; approximately one-third of them had a cystic component. Ovarian surface adhesions, involvement of the ovarian surface, or both, was present in 6% of CFs and 10% of MACFs. Eleven percent of CFs and 13% of MACFs were associated with extraovarian involvement. All tumors consisted of cellular, intersecting bundles of spindle cells with bland nuclear features. The mean highest mitotic count for MACFs was 6.7 MFs/10 HPFs (range 4 to 19 MFs/10 HPFs). Follow-up of 3 months to 12 years (mean 4.75 y) was available in 18 of the 40 patients with MACFs and was uneventful in all cases. We conclude that cellular fibromatous neoplasms with bland cytology and elevated mitotic counts are associated with favorable patient outcome and should be diagnosed as MACF rather than fibrosarcoma, which usually have moderate to severe atypia and elevated mitotic rates. As prior observations have shown that even typical CFs can occasionally recur locally, particularly if they are associated with rupture or adherence, long-term follow-up for patients with CFs and MACFs is appropriate.

(2) 子宫: 看起来是浆液性癌(endometrial intraepithelial carcinoma EIC 或者uterine serous carcinoma,需要看肿瘤大小和是否有浸润), 做个p53和p16,Ki67。EIC好发于老年人的子宫息肉。

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3 楼    发表于2010-01-21 10:49:00举报|引用
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以下是引用dujun0522在2010-1-17 11:57:00的发言:

If there is still doubt, alpha-inhibin and calretinin can settle the dispute once and for all.

卵泡膜细胞瘤和颗粒细胞瘤是不是都会表达alpha-inhibin and calretinin ?  

Yes.

Some 卵泡膜细胞瘤 can be focally positive for alpha-inhibin and calretinin. But 颗粒细胞瘤geneally are diffusely positive.  

 

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4 楼    发表于2010-01-21 10:55:00举报|引用
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 1. Agree that it is a cellular fibrothecoma.

2. Agree with Dr. Cao that ki67 and p53 stains are suggested to rule out EIC.

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5 楼    发表于2010-01-21 17:49:00举报|引用
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 子宫内膜确实是EIC,P53强阳性。
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6 楼    发表于2010-01-16 16:46:00举报|引用
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 卵巢:卵泡膜细胞瘤
内膜:息肉伴腺体潴留(鉴别腺肌瘤性息肉)
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7 楼    发表于2010-01-16 17:12:00举报|引用
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以下是引用wfbjwt在2010-1-16 16:46:00的发言:

 卵巢:卵泡膜细胞瘤
内膜:息肉伴腺体潴留(鉴别腺肌瘤性息肉)

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8 楼    发表于2010-01-16 21:40:00举报|引用
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The ovarian tumor is a cellular fibroma or fibroma/thecoma. I do not see vacuolated cytoplasm to suggest luteinization. There is no hemorrhage, necrosis, cytologic atypia or diffuse brisk mitotic activity to suggest fibrosarcoma. WHO classification of ovarian fibroma has a criterion emphasizing the importance of mitotic count; <4 mitoses/10 high-power fields is seen in benign fibroma, and >3 mitoses/10 high-power fields is seen in fibrosarcoma. It is important to note that this criterion is outdated now. In 2006 an authoritative article published in American Journal of Surgical Pathology by Young and Clement has clearly shown a category of "mitotically active cellular fibroma" among cellular fibromas that contains >3 mitoses/10 high-power fields (mostly in focal areas only and not diffuse) and remains benign in biological behavior, even in the presence of hemorrhage and necrosis. Therefore, do not diagnose ovarian fibrosarcoma unless there is atypia and the high mitotic rate is observed diffusely in a large ovarian spindle cell tumor.

The endometrial growth appears to be hyperplastic polyp with proliferative glands. Figures 48, 50, 52 and 54 display some smaller endometrial glands lined by crowded epithelia with high nucleocytoplasmic ratios that suggest focal atypia (I am not sure it is based on the photos, more would help). There is no features of invasive endometrioid adenocarcinoma or endometrial intraepithelial carcinoma of the serous type.

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9 楼    发表于2010-01-17 07:25:00举报|引用
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One differential diagnosis brought up by the case presenter is sarcomatoid granulosa cell tumor, which is why so many photos of reticulin silver stain were uploaded. Reticulin silver stain has been used to differentiate between the two - with inter- and pericellular reticulin fibrils found in fibroma/thecoma and not in granuloca cell tumor. The uploaded photos of reticulin of this case show the presence of intercellular reticulin fibrils in mant areas except for when cellularity is high and intercellular reticulin and collagen is cery scant. I believe they support the diagnosis of fibroma/thecoma and not granulosa cell tumor. Even in sarcomatois granulosa cell tumor one should be able to find traces or areas with classic features of granulosa cell tumor - oval clefted nuclei, organoid pattern, cystic change, even Call-Exner bodies. If there is still doubt, alpha-inhibin and calretinin can settle the dispute once and for all.
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10 楼    发表于2010-01-17 11:57:00举报|引用
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If there is still doubt, alpha-inhibin and calretinin can settle the dispute once and for all.

卵泡膜细胞瘤和颗粒细胞瘤是不是都会表达alpha-inhibin and calretinin ?  

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