Sabato 27 ottobre 2012 - Pacini Editore
Sabato 27 ottobre 2012 - Pacini Editore
Sabato 27 ottobre 2012 - Pacini Editore
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388<br />
an omental lymph node. To the best of our knowledge, this is the<br />
first case of LPD containing foci of lymph nodal ectopic decidua<br />
in a pregnant woman with a past history of miomectomy and use<br />
of oral contraception for three years.<br />
Methods and results. A 36 year old pregnant woman, at 38 weeks<br />
of gestation, was admitted to Garbagnate Milanese Hospital for a<br />
cesarian section. She had previously undergone miomectomy and<br />
now presented two irregular masses localized in the posterior wall<br />
of the uterus and identified during pelvic ultrasound for the monitoring<br />
of the pregnancy. The masses appeared to narrow the uterine<br />
cavity and to determine a reduced fetal growth. Past medical<br />
history of the woman revealed a miomectomy in 2007. She was<br />
using oral contraceptions for 3 years. At the time of the admission<br />
the patient was in a good condition with stable vital signs.<br />
Physical examination was unremarkable. Laboratory data were<br />
within normal limits. During the cesarian section an intraoperative<br />
biopsy at explorative laparotomy showed multiple peritoneal<br />
proliferative processes of uncertain significance. Tumors masses<br />
measured up to 6x5,5x5,5 cm and were disseminated in the majus<br />
and minus omentum. Due to the difficulties of a complete resection<br />
the surgeon decided to perform an omentectomy, preserving<br />
the uterus, to reduce the dimension of the lesions and to obtain<br />
representative tissue for histopathological examination. On gross<br />
examination, the omentum measured 21x8x12, consisted of a<br />
lobulated yellow-whitish tissue and showed multiple, firm and<br />
well circumscribed nodules. On cut section, the nodules showed<br />
white, whorled trabeculation. In the omentum a lymph node of<br />
0,5 cm in greatest diamenter was found. The histologic features of<br />
the nodules were those of typical benign uterine myomas. There<br />
was neither necrosis nor cell atypia. Mitoses were not observed.<br />
The proliferative cell index as determined by Ki-67 was about<br />
20% of the neoplastic cells. Collagen fibers were intermingled<br />
with muscle cells as well as with decidual cells scattered throughout<br />
the tumors and their periphery. Tumor cells were positive for<br />
vimentin, desmin, smooth muscle actin and muscle specific actin<br />
and strongly expressed progesterone receptors and oestrogen receptors.<br />
The omental lymph node showed foci of decidual cells,<br />
localized in the subcapsular sinus, which were loosely cohesive,<br />
with abundant eosinophilic cytoplasm, well defined prominent<br />
cytoplasmic borders and round to oval nuclei with dispersed chromatin<br />
and single conspicuous nucleoli. Immunohistochemical<br />
stains (Progesterone +, Oestrogen +, CK AE1-AE3-, CAM 5.2-,<br />
CD117-) ruled out a metastatic epithelial lesion or GIST lesions.<br />
The final diagnosis was consistent with benign tumors classified<br />
as leiomyomatosis with foci of ectopic deciduas which was also<br />
localized, peculiarly, in one of the omental lymph nodes.<br />
Discussion. We describe the case of an incidentally detected LPD<br />
with decidual foci in the tumors and in an omental lymph node in<br />
a woman with multiple risk factors for this condition: prolonged<br />
use of oral contraceptives, miomectomy and pregnancy. Several<br />
studies have illustrated the characteristics of LPD and decidual<br />
areas, their behavior and their association with other diseases but,<br />
to our knowledge, only Hsu et al have reported the association<br />
between LPD and decidua in a lymph node. LPD is difficult to<br />
diagnose due to its rarity and the possibility of mimicking malignant<br />
lesions, which are excluded in our cases in the absence<br />
of mitoses, necrosis and atypia. However, histopathological and<br />
immunohistochemical findings are diagnostic. On the other hand,<br />
the exact incidence of ectopic decidua cannot be easily estimated,<br />
because it is usually an incidental microscopic findings (in 100%<br />
of omentum biopsies taken during cesarian section and in tubal<br />
pregnancies and in 30,8% of uteri removed during pregnancy).<br />
LPD is now interpreted as an hormone-dependent lesion which<br />
can regress when hormonal stimulation has been removed. Decidual<br />
areas are frequent in LPD as well as in lymph node during<br />
pregnancy and can be related to endometriosis. It has been shown<br />
that decidua in these ectopic areas may be replaced by fibrosis.<br />
Fibroblasts may become activated as myofibroblasts and smooth<br />
CONGRESSO aNNualE di aNatOmia patOlOGiCa SiapEC – iap • fiRENzE, 25-<strong>27</strong> OttOBRE <strong>2012</strong><br />
muscle cells. The use of oral contraceptives and pregnancy can<br />
favor this metaplastic process. A metaplastic process which also<br />
involves the subperitoneal mesenchymal stem cells to smooth<br />
muscle cells, fibroblasts, myofibroblasts and decidual cells.<br />
However, in our case there were also a uterine myomectomy<br />
in the anamnesis and this does not allow to exclude a iatrogen<br />
muscle cells dissemination in the peritoneal cavity. The presence<br />
of decidual cells in the subcapsular sinus of an omental lymph<br />
node might let us hypothesize a migration of decidual cells by<br />
lymphatic vessels from the omentum to the lymph node. Post<br />
partum the patient underwent a pharmacological treatment with<br />
GnRh agonists for three months aimed at inducing a menopausal<br />
condition and reducing the residual LPD. One year post surgery<br />
the patient was well. Sonographically and in the follow-up CTscan<br />
there were no signs of persistent leiomyomatosis.<br />
references<br />
1 Al-Talib A, Tulandi T. Pathophysiology and possible iatrogenic cause<br />
of leiomyomatosis peritonealis disseminata. Gynecol Obstet Invest<br />
2010;69:239-44.<br />
2 Castro-Boix S, Dopazo-Taboada C, Nadal-Guissard A, et al. Leiomyomatosis<br />
peritonealis disseminata. Cir Esp 2007;82:125-7.<br />
3 Heinig J, Neff A, Cirkell U, et al. Recurrent leiomyomatosis peritonealis<br />
disseminata after hysterectomy and bilateral salpingo-oophorectomy<br />
during combined hormone replacement therapy. Eur j Obstet<br />
Gynecol Reprod Biol 2003;111:216-8.<br />
4 Hsu YH, et al. Leiomyomatosis in pelvic lymph node. Obstet Gynecol<br />
1981;57(6 Suppl):91S-3.<br />
5 Kumar S, Sharma JB, Verma D, et al. Disseminated peritoneal leiomyomatosis:<br />
an unusual complication of laparoscopic myomectomy.<br />
Arch Gynecol Obstet 2008;<strong>27</strong>8:93-5.<br />
6 Miyake T, Enomoto T, Veda Y, et al. A case of disseminated peritoneal<br />
leiomyomatosis developing after laparoscope-assisted myomectomy.<br />
Gynecol Obstet Invest 2009;67:96-102.<br />
7 Summa B, Schem C, Weigel M, et al. Leiomymatosis peritonealis<br />
disseminata in a pregnant woman. Arch Gynecol Obstet<br />
2010;281:123-7.<br />
8 Takeda T, Masuhara K, Kamiura S. Successful management of a<br />
leiomyomatosis peritonealis disseminata with an aromatase inhibitor.<br />
Obstet Gynecol 2008;112:491-3.<br />
9 Tavassoli FA, Norris HJ. Peritoneal leiomyomatosis (leiomyomatosis<br />
peritonealis disseminata): a clinicopathologic study of 20 cases with<br />
ultrastructural observation. Int J Gynecol Pathol 1982;1:59-74.<br />
10 Wilson JR, Peale AR. Multiple peritoneal leiomyomas associated<br />
with a granulose-cell tumor of the ovary. Am J Obstet Gynecol<br />
1952;64:204-2.<br />
Primary ovarian lymphoma: an incidental finding<br />
in two cases<br />
G. Petracco, P. Uboldi, M. Onorati, A. Del Gobbo * , S. Romagnoli<br />
* , M. Albertoni, I. Talamo, F. Di Nuovo<br />
Pathology Unit, Garbagnate Milanese, AO “G. Salvini” Garbagnate Milanese,<br />
Italy; * Department of Health Sciences, AO S. Paolo, University of<br />
Milan, Medical School, Italy<br />
Introduction. Primary ovarian lymphoma is an uncommon<br />
disease and often pose a diagnostic challenge if his existent is<br />
not suspected, because most cases of ovarian involvement by<br />
lymphomas represent secondary involvement. Most are non-<br />
Hodgkin lymphomas and constitute only the 1,5% of ovarian<br />
tumors with a prevalence ranging from 0.2% to 1.1%. It affects<br />
patients over a wide age. The peak of incidence is in the fourth or<br />
fifth decade for large B-cell lymphoma, whereas follicular lymphoma<br />
are more often found in older women. The main symptom<br />
is abdominal pain, with pelvic mass and ascites, which are also<br />
common in ovarian cancer. A minority of patients have weight<br />
loss, fatigue, fever or abdominal vaginal bleeding. Most ovarian<br />
lymphomas are large B-cell lymphomas followed by primary<br />
ovarian Burkitt’s lymphoma and follicular lymphomas. Ovarian<br />
lymphoma traditionally has been considered an aggressive tumor<br />
with a poor outcome; however in more recent reports with com-