Pathologica 4-07.pdf - Pacini Editore
Pathologica 4-07.pdf - Pacini Editore
Pathologica 4-07.pdf - Pacini Editore
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POSTERS<br />
tors may play a more important role in the angiogenesis of<br />
the latter.<br />
References<br />
1 Nakagawa T, et al. Anticancer Res 1999;19:2963-8.<br />
2 Ko SY, et al. Int J Cancer 2004;111:727-32.<br />
Neuroendocrine small cell carcinoma of the<br />
breast: a report of two cases with<br />
immunohistochemical features<br />
G. Perrone, M. Zagami, S. Morini * , G. Gullotta, V. Altomare<br />
** , C. Rabitti<br />
Anatomia Patologica, * Anatomia Umana, ** Unità di Senologia,<br />
Policlinico Universitario Campus Bio-Medico di Roma,<br />
Roma, Italia<br />
Introduction. Small cell carcinoma, although most commonly<br />
encountered in the lung, can occur in many extrapulmonary<br />
sites, including the salivary glands, upper respiratory mucosa,<br />
intestinal tract, pancreas, urinary tract, and other organs. Small<br />
cell neuroendocrine carcinoma (SCNC) a of the breast is a rare<br />
tumour with less than 30 cases reported in the literature.<br />
Case 1. A 96 year old woman presented with a mass in her<br />
right breast. Radiological and clinical examination failed to reveal<br />
tumour elsewhere in the body. She had a breast cancer excision,<br />
which was diagnosed as SCNC. The size of the tumour<br />
was 3,5 cm. Axillary clearance was not performed. Immunohistochemical<br />
study showed positivity for NSE and MNF116<br />
cytokeratin (dot-like pattern) while negative for chromogranin,<br />
synaptophysin, oestrogen receptor, progesterone receptor, p53,<br />
HER2. Ki-67 was positive in > 40% of cancer cells.<br />
Case 2. A 42 year old woman presented with a mass in her<br />
left breast. Radiological and clinical examination failed to reveal<br />
tumour elsewhere in the body. She had a simple lumpectomy<br />
with axillary dissection. Microscopically, a 3.5 cm SC-<br />
NC with focal squamous differentiation and foci of in situ<br />
ductal component with 26 negative lymph nodes was diagnosed.<br />
In the neuroendocrine small cell component, immunohistochemical<br />
study showed positivity for NSE, chromogranin,<br />
synaptophysin, MNF116 cytokeratin (dot-like pattern),<br />
while negative for HMW-CK. On the other hand, the<br />
squamous component resulted negative for NSE, chromogranin<br />
and synaptophysin while positive for MNF116 cytokeratin<br />
and HMW-CK. Furthermore, oestrogen receptor, progesterone<br />
receptor, HER2 were negative. Ki-67 and P53 were<br />
respectively positive in 98% and 50% of cancer cells.<br />
Conclusion. SCNC is a rare tumour of the breast. The distinction<br />
is particularly important in view of the perceived<br />
more aggressive behaviour 1 . The diagnosis of SCNC in the<br />
breast can usually be supported by detecting immunohistochemical<br />
evidence of neuroendocrine differentiation, however<br />
one of our cases of small cell mammary carcinoma did not<br />
display consistent immunoreactivity for neuroendocrine<br />
markers beyond strong and diffuse staining with NSE. Heterogeneous<br />
immunoreactivity for neuroendocrine markers is<br />
a well-documented observation in small cell carcinomas at<br />
other sites 2 . Demonstrating a neuroendocrine immunoprofile<br />
is supportive but not essential in rendering a diagnosis of<br />
mammary small cell carcinoma.<br />
References<br />
1 Samli B. Arch Pathol Lab Med 2000;124:296-8.<br />
2 Guinee DG. Am J Clin Pathol 1994;102:406-14.<br />
CAV-1 protein expression in lobular breast<br />
neoplasia progression<br />
M. Zagami, G. Perrone, G. Lescarini, V. Altomare * , S.<br />
Morini ** , C. Rabitti<br />
Anatomia Patologica, * Unità di Senologia, ** Anatomia<br />
Umana, Università Campus Bio-Medico di Roma, Italia<br />
Introduction. CAV-1 is the principal structural component<br />
of caveolae domains, which represent a subcompartment of<br />
the plasma membrane. Several lines of evidence suggest that<br />
caveolin-1 functions as a suppressor of cell transformation 1 .<br />
A recent report showed that expression of caveolin-1 was<br />
down-regulated in breast ductal carcinoma cells compared<br />
with the normal breast epithelial cells 2 . To data, no information<br />
exists on neoplastic lobular breast pathology. In the present<br />
study CAV-1 expression was studied in normal lobular<br />
epithelial cells, LIN lesion and in lobular invasive cancer.<br />
Materials and methods. 69 specimens of lobular neoplasm<br />
(35 LIN, 34 invasive cancers) were examined for CAV-1 expression<br />
by immunohistochemistry. CAV-1 was evaluated as<br />
percentage of positively stained cells in a total of at least<br />
1000 tumour cells. Staining for CAV-1 was considered positive<br />
if > 10% of cells were stained.<br />
Results. Immunohistochemical analysis revealed strong fine<br />
granular expression of caveolin-1 concentrated at the surface<br />
membrane and a diffuse cytoplasmic staining pattern in the<br />
normal lobular epithelial cells and surrounding endothelial<br />
cells (used as internal positive control) in all 69 cases. A<br />
strong significant difference (p < 0,0001) was found in terms<br />
of CAV-1 expression between LIN [28/35 (80%)] and invasive<br />
lesions [11/34 (32,3%)]. If CAV-1 expression was considered<br />
within different LIN grades, no significant difference<br />
was found between LIN1 and LIN2 while a significant difference<br />
was found between LIN1 and LIN3 (p = 0,02) and<br />
between LIN2 and LIN3 (p = 0,038). Moreover no significant<br />
difference was found between LIN3 and invasive lesions.<br />
Furthermore, a negative significant correlation was<br />
found between CAV-1 expression and lobular neoplasia grading.<br />
Conclusions. The higher percentage of CAV-1 positive LIN<br />
lesions compared with invasive lobular cancer and the significant<br />
negative correlation between CAV-1 expression and<br />
lobular neoplasia grading are further evidence of the possible<br />
role of CAV-1 in the development of human lobular breast<br />
cancer. Furthermore, our results show that CAV-1 expression<br />
is similar in LIN3 lesions and in invasive lobular carcinoma.<br />
A provocative possible explanation of the latter data is that<br />
LIN3, rather than LIN1 and LIN2 lesions, is a precursor lesion<br />
of invasive lobular carcinoma rather than a simple risk<br />
factor.<br />
References<br />
1 Williams TM. Mol Biol Cell 2003;14:1027-42.<br />
2 Park SS, et al. Histopathology 2005;47:625-30.<br />
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