Vol.2, No.5, 306-309 (2013) Case Reports in Clinical Medicine
http://dx.doi.org/10.4236/crcm.2013.25082
A case of kidney metastasis in vulvar squamous cell
carcinoma: A case report and review of literature
Anit a Agrawal1*, Kimberly A. Wood2, Christopher K. Giede3, Rajni Chibbar4
1Department of Obstetrics and Gynecology, University of Saskatchewan, Saskatoon, Canada;
*Corresponding Author: a.agrawal@usask.ca
2College of Medicine, University of Saskatchewan, Saskatoon, Canada
3Department of Obstetrics and Gynecology, Royal University Hospital, Saskatoon, Canada
4Department of Pathology, Royal University Hospital, Saskatoon, Canada
Received 17 December 2012; revised 25 January 2013; accepted 10 February 2013
Copyright © 2013 Anita Agrawal et al. This is an open access article distributed under the Creative Commons Attribution License,
which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
ABSTRACT
Vulvar cancer is an uncommon tumor and re-
presents 3% - 5% of all female genital tract ma-
lignancies. Squamous cell carcinoma (SCC) is
the most common carcinoma of the vulva. Dis-
t ant met astasis of recurrent vulvar squamous cell
carcinoma is rare and occurs late in the disease
process. We report the first case of kidney me-
tastasis from a vulvar squamous cell carcinoma
in a 68-year-old Caucasi an female. On initial pre-
sentation she was treated with radical vulvec-
tomy, upper urethrectomy w ith bilateral inguinal
and deep femoral lymph node dissection. She
was staged as FIGO stage IVA and also received
adjuvant chemo-radiation. She remained in re-
mission for 24 months. Subsequently she was
found to have a k idney tumor and underwent ne-
phrectomy and was diagnosed with metastatic
squamous cell carcinoma from the vulva to the
kidney. In ca ses of recur rent v ulvar carci noma dis -
t ant metastasis to the bo nes, breast, and brain is
only rarely reported. Metastasis to kidneys from
vulvar carcinoma is exceptionally rare with no
reported cases in the literature. Renal meta stas is
should be considered in the differential diagno-
sis of kidney tumor in this group of women.
Keyw ords: Vulva; Squamous Cell Carcinoma;
Kidney Metastasis
1. INTRODUCTION
Squamous cell carcinoma is the most common carci-
noma of the vulva. Squamous cell carcinoma (SCC) of
the vulva can spread via direct extension into adjacent
structures, lymphatic embolization and hematogenous
spread to distant sites [1]. Distant metastases in patients
with primary SCC of the vulva are relatively rare and
usually occur late in the disease process. In cases of re-
current vulvar carcinoma distant metastasis to bones,
breast, and brain is rarely reported. Metastasis to k idneys
from vulvar carcinoma is exceptionally rare with no re-
ported cases in the literature. Here we present the first
case of vulvar SCC with metastatic spread to the kidney.
2. CASE PRESENTATION
A 66-year-old postmenopausal woman with one year
history of lichen sclerosus et atrophicus presented in
2008 with bilateral lesions on the labia majora and mi-
nora, with ulceration present on the left labia lesion
(Figure 1). A palpable inguinal lymph node was noted on
the right side. A punch biopsy revealed moderately dif-
ferentiated keratinizin g SCC (Figure 2). Staging wo rk up
showed a single peripheral 5 mm nodule in the middle
lobe of right lung unlikely to be metastasis. Patient un-
derwent radical vulvectomy and upper urethrectomy with
bilateral inguinal and deep femoral lymph node dissec-
tion. Histopathology was consistent with an invasive
keratinizing SCC with a 5 mm depth of invasion. Ure-
thral and deep vagina margins were focally positive with
carcinoma. One out of six and 1 out of 5 inguinal lymph
nodes were positive for metastatic spread on the left and
right side respectively. Deep femoral lymph nodes on the
left side were positive (2/2). She was staged as FIGO
stage IVA (pT3 pN3 M0 G2). The patient underwent con-
current chemo-radiation therapy consisting of cisplatin
and external beam radiotherapy of a 4500 cGy in 25
fractions o ve r 3 6 day s.
Patient remained in remission for 24 months and in
2010 experienced sudden onset of severe left flank pain
and microscopic hematuria. CT scan of the abdomen
Copyright © 2013 SciRes. OPEN A CCESS
A. Agrawal et al. / Case Reports in Clinical Medicine 2 (2013) 306-309 307
Figure 1. Vulvar tumor on initial presentation.
Figure 2. High power H & E stain vulvar tumor showing high
grade squamous cell carcinoma.
reported a 5.5 × 4.5 × 4.5 cm infiltrative, ill defined,
solid heterogeneous exophytic mass present within the
left kidney appearance suggestive of renal cell carcinoma
(Figure 3). Low density adenopathy was present subjacent
to renal vein, measuring 2.2 cm. A left radical nephrec-
tomy and para-aortic lymph dissection was performed.
Gross examination of the left kidney revealed two
masses, one extended through the capsule to the perirenal
fat and into the renal sinus and measured 5.5 × 4.5 × 4.5
cm and the other was present in the upper pole of the
perirenal fat and measured 1.0 × 0.8 × 0.9 cm. Micro-
scopic examination revealed moderately differentiated
keratinizing SCC with lympho-vascular invasion consis-
tent with metastatic vulvar carcinoma (Figure 4). Me-
tastatic disease was also noted in the para-aortic lymph
nodes (Figure 5) and small foci within the renal paren-
chyma and perirenal fat.
The patient’s health progressively declined and was
transferred to palliative care unit and passed away 2
weeks later in 2010.
Figure 3. CT scan showing a 5.5 cm left renal tumor and en-
larged para-aortic lymph nodes.
Figure 4. Low power H & E stain kidney showing metastatic
vulvar squamous cell carcinoma.
Figure 5. High power H & E stain lymph node showing me-
tastatic vulvar squamous cell carcinoma.
3. DISCUSSION
Carcinoma of the vulva represents 3% to 5% of all
female genital tract malignancies and 90% of the primary
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A. Agrawal et al. / Case Reports in Clinical Medicine 2 (2013) 306-309
308
vulvar malignancies are diagnosed as SCC [1]. Vulvar
SCC can spread by three different routes, direct exten-
sion to adjacent structures, lymphatic embolization and
hematogenous spread to distant sites. Lymphatic spread
occurs early in the disease process and will commonly
spread to the ipsilateral inguinal, femoral and pelvic
lymph nodes, in a sequential manner. Spread to the in-
guinal and femoral lymph nodes occurs in about 30% of
the patients and about 12% of patients will have spread
to the pelvic lymph nod es.
Hematogenous spread to distant sites varies and occurs
in about 8% - 1 2% of patients [2]. Distan t sites of spread
were reported in lung [3,4], skin [4-7], bone [4,8], intra-
abdominal [4], liver [4], heart [4], breast [9], muscle [2]
and central nervous system [4,10,11]. Our case is un ique
in that distant metastatic spread occurred to the kidney,
which has not been previously reported in literature.
Metastatic spread of cancer to the kidneys is not
common despite the fact that the kidneys receive 20% of
the cardiac output. Metastatic spread to the kidney usu-
ally occurs through a combination of venous and lym-
phatic routes. Autopsy findings showed that the most
common metastatic renal lesion is lymphoma [12] and
the top four carcinomas metastasizing to the kidneys are
lung, breast, stomach and opposite kidney [11,12] occur-
ring in 4.6% to 7.6% of patients [13].
Majority of patients presenting with metastatic spread
to the kidneys are asymptomatic and the presence of the
kidney metastasis are not known un til autopsy. However,
patients with renal metastases may present with albu-
minuria, microscopic hematuria, a renal mass or renal
failure [14]. In this case, the patient was diagnosed with
a kidney metastasis after presenting to the emergency
department with severe flank pain and microscopic he-
maturia. A CT scan confirmed the presence of a solid
mass in the left kidney and a radical nephrectomy was
performed.
4. CONCLUSION
Although renal metastasis is rare, and has never been
documented in a case of vulvar SCC, it should be con-
sidered in the differential diagnosis of flank pain and
microscopic hematuria in women with a past history of
vulvar carcinoma. To the best of our knowledge, this is
the first reported case of vulvar carcinoma which devel-
oped renal metastasis.
5. RESULTS
We report a case of 68-year-old women who were
treated in September 2008 with radical vulvectomy, dis-
tal uretherectomy, and bilateral inguinofemoral lympha-
denectomy for FIGO stage IVA (pT3 pN3, M0 G2) mod-
erately differentiated squamous cell vulvar carcinoma.
Due to a positive bilateral lymph node status, close
vaginal and urethral margin, she received adjuvant pelvic
and vulvar radiation (4500 cGy).
The patient remained clinically in remission until Oc-
tober 2010, when presented with flank pain. CT scan of
abdomen reported a 5.5/4.5/4.5 cm tumor in the left kid-
ney and appearance was suggestive of renal cell carci-
noma (Figure 1). A left radical nephrectomy including
paraaortic lymph node dissection was performed in No-
vember 2010. The histopathology and of resected renal
tumor and paraaortic lymph nodes gave evidence of a
metastasis of the known vulvar carcinoma.
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