Skip Navigation

This Article
Right arrow Abstract Freely available
Right arrow FREE Full Text (PDF) Freely available
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (10)
Right arrow Request Permissions
Google Scholar
Right arrow Articles by Kubo, M.
Right arrow Articles by Hasegawa, T.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Kubo, M.
Right arrow Articles by Hasegawa, T.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Japanese Journal of Clinical Oncology 31:510-513 (2001)
© 2001 Foundation for Promotion of Cancer Research

Association of Breast Cancer with Meningioma: Report of a Case and Review of the Literature

Makoto Kubo1, Takashi Fukutomi1, Sadako Akashi-Tanaka1 and Tadashi Hasegawa2,+

1Breast Surgery Division, National Cancer Center Hospital, Tokyo and 2Pathology Division, National Cancer Center Research Institute, Tokyo, Japan


    ABSTRACT
 TOP
 ABSTRACT
 INTRODUCTION
 CASE REPORT
 DISCUSSION
 REFERENCES
 
We report a case of meningioma subsequently developed in a patient with primary breast carcinoma. A 53-year-old woman received a left modified radical mastectomy because of stage IIA breast carcinoma. Histologically, the tumor was a predominantly intraductal carcinoma with negative lymph node metastasis. Estrogen receptor (ER) was negative but progesterone receptor (PR) of the left tumor was positive by immunohistochemistry. Four years later, cranial bone and/or brain metastasis was suspected from a routine follow-up bone scintigram. The patient showed no symptoms or signs at that time. Magnetic resonance imaging (MRI) and angiography revealed that the right parasagittal mass was suspicious of meningioma. A complete tumor removal was performed. On histological examination, this brain tumor was a transitional-type meningioma (meningotheliomatous and fibrous type) without malignant findings. ER was negative but PR was positive also in this tumor. She is currently well 6 years after the initial surgery. A review of the literature is presented with emphasis on the association between breast cancer and meningioma, which indicates a possible hormonal relationship. The knowledge of this association is important in the differential diagnosis of patients with breast cancer who develop central nervous manifestations.


    INTRODUCTION
 TOP
 ABSTRACT
 INTRODUCTION
 CASE REPORT
 DISCUSSION
 REFERENCES
 
It has been reported that the incidence of meningioma is increased in patients with breast cancer (1). The increased risk of developing meningioma was reported to be 1.57–1.90 times after breast cancer according to data from the Swedish Cancer Registry and from the United States Surveillance, Epidemiology and End Results (SEER) Program (2,3). It is therefore important to differentiate a solitary brain metastasis from a meningioma, which is a potentially curable disease. Hormonal relationships between meningioma and breast cancer have also been suggested (4,5). The pregnancy and/or menstrual cycle is sometimes related to the rapid increase of meningiomas (6). We report here a case of meningioma subsequently developed in a patient with primary breast carcinoma.


    CASE REPORT
 TOP
 ABSTRACT
 INTRODUCTION
 CASE REPORT
 DISCUSSION
 REFERENCES
 
A 53-year-old postmenopausal woman with a left primary breast carcinoma (T2N0M0: stage IIA) was referred to our hospital. She had no past or family history of malignancies. The tumor size was 3.1 cm in diameter at the first consultation. As for the diagnostic procedures, mammography (MMG: Mammomat 3, Siemens, Germany) revealed an ill-defined, spiculated tumor shadow with diffuse microcalcifications in the left breast. An irregular hypoechoic–tumorous lesion could be detected in the upper-outer quadrant of the left breast by ultrasonography (US: EUB-515 with a 7.5 MHz transducer; Hitachi, Tokyo, Japan). A modified radical mastectomy of the left breast was carried out in July 1995. Histological examination revealed that the left breast tumor was a predominantly intraductal carcinoma, histological grade 3, with negative lymph node metastasis (0/14) (Fig. 1). Estrogen receptor (ER) was negative but progesterone receptor (PR) of this tumor was positive by immunohistochemistry (Fig. 2). Whereas the size of the invasive component was only 1.7 x 1.0 cm in diameter (20%), the size of the intraductal component was 6.2 x 3.0 cm in diameter (80%). Lymphatic invasion by tumor cells was negative but vascular invasion by tumor cells was positive. Positive p53 nuclear immunoreaction (RSp53, Nichirei, Tokyo, Japan) and strongly positive HER-2 overexpression (Dako Japan, Tokyo, Japan) by immunohistochemical staining were observed in this tumor. No adjuvant chemotherapy was given to the patient. Four years later, cranial bone and/or brain metastasis was suspected from a routine follow-up bone scintigram. The patient showed no symptoms or signs at that time. No other metastatic lesion was detected by abdominal ultrasonography and chest X-ray. Bone X-ray of the skull revealed no abnormalities. Magnetic resonance imaging (MRI) demonstrated a circumscribed lesion in the right parasagittal region with low signal intensity on T1-weighted imaging and with weakly high intensity on T2-weighted imaging. The tumor was homogeneously enhanced by gadolinium, whereas a metastatic tumor is not homogeneously enhanced. Angiography demonstrated a hypervascular mass in the same region. These imagings revealed that the tumor was suspicious of meningioma of the right parasagittal region. However, there was a possibility of a solitary brain metastasis. Tumor markers (CEA, CA15-3, ST-439) were all within the normal ranges. A complete tumor removal was performed in June 2000. Histologically, this brain tumor was composed of spindle cell proliferation and increasing collagen bundles. It was a transitional-type meningioma (meningotheliomatous type and fibrous type) without malignant findings (Fig. 3). ER was negative but PR was positive also in this tumor (Fig. 4). The patient is currently well 6 years after the initial surgery for breast cancer.



View larger version (151K):
[in this window]
[in a new window]
 
Figure 1. Histopathological examination of the left breast tumor.

 


View larger version (120K):
[in this window]
[in a new window]
 
Figure 2. Immunohistochemical examination of the left breast cancer by progesterone receptor (PR).

 


View larger version (141K):
[in this window]
[in a new window]
 
Figure 3. Histopathological examination of the brain tumor.

 


View larger version (133K):
[in this window]
[in a new window]
 
Figure 4. Immunohistochemical examination of the meningioma by PR.

 

    DISCUSSION
 TOP
 ABSTRACT
 INTRODUCTION
 CASE REPORT
 DISCUSSION
 REFERENCES
 
We have two other patients with probable meningiomas subsequently developed after primary breast carcinoma. One of these two breast cancers was PR-positive despite the lack of ER, just as in the present case. Course observation was selected for these two patients because of the meningioma-like masses with stable size by imaging modalities and no symptoms or signs. Also seven (8.3%), including this patient, of 84 patients whose meningiomas were removed at our hospital from May 1981 to June 2000 had undergone surgical treatment for breast cancer. The remaining six patients except for this one had been treated at another hospital. Therefore, the data were not available in detail. The clinicopathological characteristics of the three patients with breast cancer and meningioma treated at our hospital are summarized in Table 1.


View this table:
[in this window]
[in a new window]
 
Table 1. Clinicopathological features of three breast cancers in patients with meningioma
 
It has been reported that breast cancer is the second most common cause of intracranial metastases (4). We previously reported seven cases of breast cancer recurrence limited to the central nervous system (CNS) without other visceral metastases (5). In that study, premenopausal patients with negative hormone receptor status were more likely to develop this kind of recurrence, regardless of the histological type.

As we reported here, a patient who has symptoms and signs suggesting a space-occupying lesion of the central nervous system after treatment for breast cancer does not always have brain metastases. Many case reports have suggested an association between breast cancer and meningioma (1,4,79). On the other hand, Backhouse et al. reported a case with optic nerve breast cancer metastasis mimicking meningioma (10).

Meningiomas occur twice as frequently in women as in men (4). In addition, some of the meningiomas were reported to express more PRs than ERs (11). Grunberg et al. reported the usefulness of anti-progesterone for recurrent meningiomas (12). Rona et al. reported that 64% of 33 meningiomas examined showed some level of progesterone receptor messenger RNA expression with which the immunohistochemistry data correlated well (13). Also, the resected meningioma in this report expressed weakly positive PRs in spite of the ER negativity, just like the hormone receptor status of the primary breast cancer in the present patient. Blankenstein et al. reported estrogen receptor-independent expression of progesterone receptor in human meningioma (14). Only one group described the ER and PR status of both breast cancer and meningioma of nine patients who developed meningioma diagnosed by surgical materials after resection of breast cancers (15). They reported two initial breast cancers and four subsequent meningiomas in nine of their cases that were positive for PR assay. In their report, all patients were alive after 1–11 years follow-up. Based on these findings, a hormonal interrelationship, particularly progesterone, is suggested for breast cancers and meningiomas. Meanwhile, alterations of the BRCA1 and BRCA2 genes are not common pathogenetic events in the development of meningiomas (16). There was no evidence for PTEN mutations in families with breast cancer and brain tumors (17). Further studies will be required to clarify the hormonal relationships between breast cancers and meningiomas.

The onset and types of neurological symptoms of metastatic breast cancer and intracranial meningioma are so similar that it is difficult to differentiate them (15). As in this case, Lee et al. documented two meningiomas detected incidentally by bone scintigraphy (18). Computed tomography (CT), magnetic resonance imaging (MRI) and angiography may be the useful diagnostic imaging modalities for this type of tumor (15,19). It is important to differentiate a CNS metastasis from a meningioma, which is a curable condition.


    FOOTNOTES
 
+ For reprints and all correspondence: Takashi Fukutomi, Department of Surgical Oncology, National Cancer Center Hospital, 1–1, Tsukiji 5-chome, Chuo-ku, Tokyo 104-0045, Japan Back


    REFERENCES
 TOP
 ABSTRACT
 INTRODUCTION
 CASE REPORT
 DISCUSSION
 REFERENCES
 
1 Smith FP, Slavik M, MacDonald JS. Association of breast cancer with meningioma. Cancer 1978;42:1992–4.[Web of Science][Medline]

2 Malmer B, Tavelin B, Henriksson R, Grönberg H. Primary brain tumors as second primary: a novel association between meningioma and colorectal cancer. Int J Cancer 2000;85:78–81.[Web of Science][Medline]

3 Ahsan H, Neugut AI, Bruce J. Association of malignant brain tumors and cancers of other sites. J Clin Oncol 1995;13:2931–5.[Abstract]

4 Rubinstein AB, Schein M, Reichenthal E. The association of carcinoma of the breast with meningioma. Surg Gynecol Obstet 1989;169:334–6.[Web of Science][Medline]

5 Higashi H, Fukutomi T, Watanabe T, Adachi I, Narabayashi M, Shibui S, et al. Seven cases of breast cancer recurrence limited to the central nervous system without other visceral metastases. Breast Cancer 2000;7:153–6.[Medline]

6 Bickerstaff ER, Small JM, Guest IA. The relapsing course of certain meningiomas in relation to pregnancy and menstruation. J Neurol Neurosurg Psychiatry 1958;21:89–91.

7 Mehta D, Khatib R, Patel S. Carcinoma of the breast and meningioma. Cancer 1983;51:1937–40.[Web of Science][Medline]

8 Burn PE, Jha N, Bain GO. Association of breast cancer with meningioma. A report of five cases. Cancer 1986;58:1537–9.[Web of Science][Medline]

9 Jacobs DH, McFarlane MJ, Holmes FF. Female patients with meningioma of the sphenoid ridge and addition primary neoplasms of the breast and genital tract. Cancer 1987;60:3080–2.[Web of Science][Medline]

10 Backhouse O, Simmons I, Frank A, Cassels-Brown A. Optic nerve breast metastasis mimicking meningioma. Aust NZ J Ophthal 1998;26:247–9.[Web of Science][Medline]

11 Blankenstein MA, Verheijen FM, Jacobs JM, Donker TH, van Dujinhoven MW, Thijssen JH. Occurrence, regulation and significance of progesterone receptors in human meningioma. Steroids 2000;65:795–800.[Web of Science][Medline]

12 Grunberg SM, Weiss MH, Spitz IM, Ahmadi J, Sadun A, Russell CA, et al. Treatment of unresectable meningiomas with the antiprogesterone agent mifepristone. J Neurosurg 1991;74:861–6.[Web of Science][Medline]

13 Rona SC, Danuta G, Kathleen D, Peter MB. Progesterone receptor expression in meningiomas. Cancer Res 1993;53:1312–6.[Abstract/Free Full Text]

14 Blankenstein MA, Koehorst SG, van der Kallen CJ, Jacobs HM, van Spiel AB, Donker GH, et al. Oestrogen receptor independent expression of progestin. Biochem Mol Biol 1995;53:361–5.

15 Salvati M, Cervoni L. Association of breast carcinoma and meningioma: report of nine new cases and review of the literature. Tumori 1996;82:491–3.[Web of Science][Medline]

16 Kirsh M, Zhu JJ, Black PM. Analysis of the BRCA1 and BRCA2 genes in sporadic meningiomas. Genes Chromosom Cancer 1997;20:53–9.[Web of Science][Medline]

17 Lauge A, Lefebre C, Laurent-Puig P, Caux V, Gad S, Eng C, et al. No evidence for germline mutations in families with breast and brain tumors. Int J Cancer 1999;84:216–9.[Web of Science][Medline]

18 Lee GK, Coel M, Ko J, Tom B. Two meningiomas detected incidentally by Tc-99m HDP bone scitigraphy during a work-up for breast cancer. Clin Nucl Med 1999;24:525–6.[Web of Science][Medline]

19 Markopoulos CH, Sampalis F, Givalos N, Gogas H. Association of breast cancer with meningioma. Eur J Surg Oncol 1998;24:332–4.[Web of Science][Medline]

Received April 9, 2001; accepted July 4, 2001.


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
The OncologistHome page
M. D. Tabernero, A. B. Espinosa, A. Maillo, O. Rebelo, J. F. Vera, J. M. Sayagues, M. Merino, P. Diaz, P. Sousa, and A. Orfao
Patient Gender Is Associated with Distinct Patterns of Chromosomal Abnormalities and Sex Chromosome Linked Gene-Expression Profiles in Meningiomas
Oncologist, October 1, 2007; 12(10): 1225 - 1236.
[Abstract] [Full Text] [PDF]


This Article
Right arrow Abstract Freely available
Right arrow FREE Full Text (PDF) Freely available
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (10)
Right arrow Request Permissions
Google Scholar
Right arrow Articles by Kubo, M.
Right arrow Articles by Hasegawa, T.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Kubo, M.
Right arrow Articles by Hasegawa, T.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?