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    <title>IMC Journal of Medical Science</title>
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                <title><![CDATA[Large Cell Neuroendocrine Cancer (LCNEC) of uterine cervix]]></title>

                                    <author><![CDATA[Gehanath Baral]]></author>
                                    <author><![CDATA[Reetu Sharma]]></author>
                
                <link data-url="https://imcjms.com/public/registration/journal_full_text/137">
    https://imcjms.com/public/registration/journal_full_text/137
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                <pubDate>Sun, 06 Nov 2016 14:27:37 +0000</pubDate>
                <category><![CDATA[Clinical Case Report]]></category>
                <comments><![CDATA[Ibrahim Med. Coll. J. 2009; 3(1): 36-38]]></comments>
                <description>Ibrahim Med. Coll. J. 2009; 3(1): 36-38
Key
words: Uterine cervix,
neuroendocrine cancer (NEC), human papilloma virus (HPV)
Introduction
Large
cell neuroendocrine carcinoma (LCNEC) of the uterine cervix is a very rare
malignancy (less than 5% of all cervical malignancies) that is highly
aggressive with unfavorable outcomes.1,2&amp;nbsp;These tumors have been classified into four
categories: small cell, large cell, classic carcinoid, and atypical carcinoid.
Most patients with early stage disease develop metastasis. Frequent metastatic
sites include the central nervous system, lung, and bone.3&amp;nbsp;Despite aggressive surgical
therapy, even in early-stage patients, mortality is high. This propensity for
rapid, local and distant spread in early-stage disease emphasizes the need for
systemic treatment.2&amp;nbsp;In some
cases, the initial diagnosis maybe confused with either poorly differentiated
squamous- or adeno-carcinomas.3
Case history
A 45
year old, grandmultipara, whose last childbirth was 5 years ago, came to ObGyn
OPD, for the first time, from a remote area of Nepal, in September 2005. She
had a history of irregular bleeding and whitish discharge per vagina since last
6-7 months. She had no other complain. On pelvic examination, there was a
growth of 4x4 cm, arising
from the posterior lip of the cervix. The growth was soft and bled on touch.
Uterine size was normal, no parametrial thickening and no palpable adnexal
masses could be palpated. She was advised to have diagnostic biopsy which she
declined. She however came back after five months and was advised to undergo
biopsy which she denied but opted for a total abdominal hysterectomy with
bilateral salpingo-oophorectomy. Part of the parametrium was also excised along
with the uterus which looked grossly normal. There was no ascites, no
abnormality in abdominal visceras and no palpable lymph nodes. Uterine body,
tubes and ovaries looked normal. Post operative period was uneventful.
Results
Grossly, on cut section, the tumor showed a yellowish white mass
located in the posterior lip of cervix, measuring approximately 4 cm in
diameter with gray white areas (Figure 1). Tissues were sectioned, stained with
hematoxyllin and eosin and evaluated under light microscopy. Sections showed
tissue lined by stratified squamous epithelium (Figure 2). Underlying stroma
showed a tumor composed of malignant cells arranged in clusters, trabeculae,
insular pattern, and solid sheets. The cells showed pallisading at the
periphery of the clusters (Figure 3). Clear cleft like retraction spaces were
seen around the cell clusters. At some areas the cells were arranged around
blood vessels. At several foci the cells formed numerous rosettes and pseudo
rosettes (Figure 4). The cells showed moderate cytoplasm with oval to round
nuclei with mild pleomorphism and fine to coarse chromatin. Atypical mitotic
figures were observed. The criterion used to diagnose the disease entity was, a
tumor of the uterine cervix composed of relatively uniform medium to large
cells exhibiting neuroendocrine differentiation apparent by light microscopy,
as evidenced by trabecular or insular arrangements of the cells, eosinophilic
cytoplasmic granules of the type seen in neuroendocrine cells, or both of these
features.4&amp;nbsp;Thus
the histopathological diagnosis was “large cell type of neuroendocrine cancer
of uterine cervix and surgical margins free of tumor.”
&amp;nbsp;
Fig-2. Adjacent
stratified squamous epithelium of the ectocervix (10X, hematoxyllin and eosin stain)
&amp;nbsp;
 Perivascular pseudo
rosettes
&amp;nbsp;
&amp;nbsp;Discussion
Large
cell neuroendocrine carcinoma (LCNEC) of the uterine cervix is a rare
malignancy that is highly aggressive and usually results in unfavorable
outcomes. They are rarely discovered on routine Pap smear due to the submucosal
location of the tumor with intact overlying mucosa in its earlier stages. The
5-year survival rate is similar to that of small cell type i.e. 14-39%.5
Early
cases are asymptomatic. Usual presentation will be irregular vaginal bleeding,2&amp;nbsp;postcoital vaginal spotting
and sanguineous vaginal discharge. Pelvic examination may reveal either
cervical erosion or a cervical growth. It is quite possible that LCNECsare frequently misdiagnosed as poorly differentiated squamouscell carcinomas or poorly differentiated adenocarcinomas, basedupon the identification of focal areas of squamous or glandulardifferentiation, respectively.3,6,7&amp;nbsp;In such cases, the subtleneuroendocrine features of the large cell neoplasm are easilyoverlooked. In such cases neuroendocrine markers will be of help.
Early-stage
large cell neuroendocrine tumors of the cervixareag gressiveun likes quamouscell carcinomas. Multimodal therapy should be
considered at the time of initial diagnosis. Based on the rarity of cervical
neuroendocrine tumors it is difficult to perform large-scale randomized control
trials to delineate optimal therapy. Therefore, the basis for treatment of
large cell neuroendocrine tumors is derived from therapy for small cell
cervical carcinoma and small cell lung carcinoma.2,3&amp;nbsp;Due to the rarity of this
tumor even in pulmonary LCNEC, the incidence, prognosis and optimal treatment
remain undetermined.8-10&amp;nbsp;Large
cell neuroendocrine tumors of the cervix are uncommon, and typically the
patients have a poor prognosis. Disease recurrences are frequent and distant
metastasis is common.2,9&amp;nbsp;Frequent metastatic sites include the central
nervous system, lung and bone.
Conclusion
Our case
study reports that LCNEC may present as a bleeding cervical polyp. It should be
interpreted carefully on histopathology so that it is not misdiagnosed as
poorly differentiated carcinoma of cervix. Since LCNEC is an aggressive tumor,
multimodality treatment is advised for the benefit of the patient to reduce
mortality.
Acknowledgement
&amp;nbsp;
1.&amp;nbsp;&amp;nbsp; Tsou MH, Tan TD, Cheng
SH, Chiou YK. Small cell carcinoma of the uterine cervix with large cell
neuroendocrine carcinoma component. Gynecol Oncol 1998; 68(1):
69-72.
3.&amp;nbsp;&amp;nbsp; Krivak TC, McBroom JW,
Sundborg MJ, Crothers B, Parker MF. Large cell neuroendocrine cervical
carcinoma: a report of two cases and review of the literature. Gynecol Oncol
2001; 82(1): 187-91.
5.&amp;nbsp;&amp;nbsp; WHO classification of
tumors. Tumors of the Breast and Female Genital Organs. 2003.
7.&amp;nbsp;&amp;nbsp; Sato Y, Shimamoto T,
Amada S, Asada Y, Hayashi T. Large cell neuroendocrine carcinoma of the uterine
cervix: a clinicopathological study of six cases. Int J Gynecol Pathol 2003;
22(3): 226-30.
9.&amp;nbsp;&amp;nbsp; Tangjitgamol S,
Manusirivithaya S, Choomchuay N, Leelahakorn S, Thawaramara T, Pataradool K, et
al. Paclitaxel and carboplatin for large cell neuroendocrine carcinoma of the
uterine cervix. J Obstet Gynaecol Res 2007; 33(2): 218-24.
11.Albores-Saavedra J,
Gersell D, Gilks CB, Henson DE, Lindberg G, Santiago H, et al. Terminology of
endocrine tumors of the uterine cervix: results of a workshop sponsored by the
College of American Pathologists and the National Cancer Institute. Arch
Pathol Lab Med 1997; 121(1): 34-9.</description>

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