Acta Dermato-Venereologica 99-7CompleteContent | Page 21
SHORT COMMUNICATION
691
Evaluation of Sentinel Lymph Node Biopsy for Eccrine Porocarcinoma
Kanako TSUNODA 1 *, Masazumi ONISHI 1 , Fumihiko MAEDA 1 , Toshihide AKASAKA 2 , Tamotsu SUGAI 3 and Hiroo AMANO 1 *
Department of Dermatology, Iwate Medical University School of Medicine, 19-1 Uchimaru, Morioka, Iwate 020-8505, 2 Department of
Dermatology, Kitakami Saiseikai Hospital, Iwate, and 3 Department of Molecular Diagnostic Pathology, School of Medicine, Iwate Medical
University, Morioka, Japan. E-mail: [email protected]; [email protected]
1
Accepted Mar 13, 2019; E-published Mar 14, 2019
Eccrine porocarcinoma (EPC) is a sweat gland carcinoma
thought to arise from the lower portion of intraepidermal
eccrine ducts. This tumour is rare (0.005–0.01% of all ma-
lignant skin tumours) (1) and information about its biological
behaviour is limited, although it is known to be aggressive.
Previous studies have reported that the local recurrence rate is
17–20% (2), the regional lymph node (RLN) metastasis rate
20%, and the distant metastasis rate 11% (3). In patients who
have RLN metastasis, the prognosis is poor, with a mortality
rate of 65% (4). In EPC, the lymphogenous route is thought to
be the main initial metastatic pathway, and therefore it can be
reasonably expected that the prognosis would be improved by
sentinel lymph node (SLN) biopsy, discovery of early lymph
node metastasis, and RLN dissection. However, few case
reports have documented the use of SLN biopsy in patients
with EPC, and no large-scale studies have been conducted.
Our department has been conducting SLN biopsy for EPC
since 2009, and during this period we have accumulated 13
surgical cases of EPC. This paper reviews these cases, to-
gether with previous reports of EPC, and discusses the use
of SLN biopsy for this malignancy and future issues.
PATIENTS, METHODS AND RESULTS
Between 2009 and 2017, 13 patients were diagnosed as having
EPC at the Department of Dermatology, Iwate Medical University,
Iwate, Japan. Pathologically, the tumours showed malignant charac-
teristics, such as irregular structures, invasive growth and unclear
borders. They consisted of atypical poroid cells with dark basaloid
staining and cuticular cells with eosinophilic staining. Duct struc-
tures were also evident. The tumour cells were immunopositive for
carcinoembryonic antigen (CEA) and/or epithelial membrane anti-
gen (EMA). SLN biopsy was performed for cases in which lymph
node/distant metastasis was not recognized by imaging (computed
tomography (CT) and/or positron emission tomography – computed
tomography (PET – CT)) before surgery. On the other hand, SLN
biopsy was not performed for cases in which metastasis to RLN
was clear or obvious based on preoperative imaging examination;
instead, immediate RLN dissection was performed in all such cases.
For identification of SLN, the radioisotope (RI) method and
indocyanine green (ICG) fluorescence method were used together.
A detailed description of the SLN is shown in Appendix S1 1 .
Among the 13 cases, only one was treated by simple wide
resection of the primary tumour. The patient was elderly and did
not wish to undergo SLN biopsy, opting for minimally invasive
surgery. Clinical and imaging findings before surgery demonstrated
no lymph node metastasis, and SLN biopsy was performed in 8
cases. Among them, 3 cases were positive for SLN metastasis
(positivity rate 37.5%). In 4 cases where clinical and/or imaging
examinations revealed RLN metastasis, dissection of the affected
https://www.medicaljournals.se/acta/content/abstract/10.2340/00015555-3173
1
nodes was performed at initial surgery (Fig. S1 1 ). The characte-
ristics of each treatment group are shown in Table SI 1 . The clini-
copathological features of SLN biopsy metastasis-negative cases
are shown in Table SII 1 and those of positive cases in Table SIII 1 .
RLN dissection was performed in all 3 patients who were positive
for SLN metastasis. The mean observation period was 28.7 months
and, at time of writing, all of the 3 patients are currently alive.
In one patient (Case 1 in Table SIII 1 ), recurrence was observed
in the parotid gland at 22 months, and resection was performed.
The mean Ki-67 labelling index in the SLN metastasis-negative
group (n = 5) was 16.6% (Table SI 1 ), and none of the patients in
this group had vascular or lymphatic invasion (Table SII 1 ). On the
other hand, the mean Ki-67 labelling index in the SLN metastasis-
positive group (n = 3) was high (21.0%) (Table SI 1 ), and vascular
and lymphatic invasion was observed in 2 of the 3 patients in
this group (Table SIII 1 ). For all SLN metastasis-positive cases,
postoperative chemotherapy was administered. The regimen for
postoperative chemotherapy was cisplatin (60 mg/m 2 ) and doxoru-
bicin (Adriamycin) (30 mg/m 2 ) once a month. The regimen was
based on that used for advanced squamous cell carcinoma (SCC).
However, continuation of this regimen is likely to cause bone mar-
row suppression, kidney damage, and cardiotoxicity. Therefore,
it can be administered for only 3 cycles. There were no serious
side-effects, however. In case number 2 (Table SIII 1 ), the patient
requested to be administered only one cycle. Table SIV 1 shows
the clinicopathological features of the RLN dissection group. The
mean observation period was 30.7 months. All patients in the RLN
dissection group had lymphatic invasion. In addition, the mean Ki-
67 labelling index was as high as 32.3% (Table SI 1 ). Postoperative
chemotherapy was administered to all 4 of the patients, but 2 of
them died due to multiple distant metastasis. The primary regimen
for postoperative chemotherapy was cisplatin and Adriamycin
once a month. The dose is described above. For patients showing
a poor treatment response, docetaxel (60 mg/m 2 ) was administered
monthly, and if this proved ineffective, irinotecan (100 mg/m 2 )
was administered on days 1, 8 and 15, and then every 4–5 weeks.
After surgery, the levels of tumour markers (CEA and CYFRA)
were checked monthly and CT imaging examinations performed
every 3 months in all patients with EPC. However, if elevation of
a tumour marker was evident, imaging was carried out promptly.
DISCUSSION
The utility of SLN biopsy for staging of malignant mela-
noma and breast cancer has been well established (5, 6). Re-
cently, SLN biopsy has also been attempted for patients with
non-malignant melanoma, such as SCC and extramammary
Paget’s disease, in which the lymphoid route is thought to be
the predominant metastatic pathway. Lymphatic metastasis
is also believed to be the main mode of metastasis in EPC.
We believe that to improve the prognosis of patients with
EPC, it is important to perform SLN biopsy for identification
of lymph node metastasis at an early stage and to perform
RLN dissection in positive cases. However, few case reports
of EPC have documented the use of SLN biopsy.
This is an open access article under the CC BY-NC license. www.medicaljournals.se/acta
Journal Compilation © 2019 Acta Dermato-Venereologica.
doi: 10.2340/00015555-3173
Acta Derm Venereol 2019; 99: 691–692