Eur Surg (2012) 44/4: 255–266
Printed in Austria
DOI 10.1007/s10353-012-0098-3
© Springer-Verlag 2012
Sacrococcygeal Teratoma – a single center study
of 43 years (1968 – 2011) including follow-up data
and histopathological reevaluation of specimens
Th. Hager
2,3
, C. Sergi
2
, J. Hager
1
1
Department of Pediatric Surgery, Medical University of Innsbruck, Innsbruck, Austria
2
Institute of Pathology, Medical University of Innsbruck, Innsbruck, Austria
3
Institute of Pathology and Neuropathology, University Hospital of Essen, University Duisburg-Essen,
Essen, Germany
Received March 20, 2012; accepted after revision May 10, 2012
Summary. Background: Sacrococcygeal teratomas
(SCTs) are neoplasms, which are mostly categorized as
benign at birth. If not resected short after birth, malignant
transformation can occur in a timely manner. Moreover,
timely resected and benign classified SCTs may reoccur
years later as malignant relapse. Finally SCTs can cause
several intrauterine and/or postoperative complications
which can alter the patients for lifetime.
Methods: Between January 1968 and December
2011 29 children underwent surgical interventions due
to SCT at our Department. One additional, primarily
outward treated girl was operated due to a malignant
relapse. Clinical records of 24 patients (all survived) and
of the girl with the relapse (who died 7 months after
second intervention) were accessible. A complete clinical
follow-up including optional multidisciplinary examina-
tions was carried out, possible in 16 patients, of whom
one girl had malignant relapse. A comparison among
three of the most common histological classifications of
SCT was made using the histology available of the 25
mentioned patients.
Results: Except for incontinence problems in four
patients and dissatisfaction with scar formation in 5
cases, the results were surprisingly good. Histological
reevaluation showed no differences between the
classifications.
Conclusions: Despite the heterogeneity of treatment
within the last 43 years, all 24 “own” patients survived.
The 16 re-examined patients showed no significant com-
plaints. Histological grading of SCTs is comparable even
using different classification systems and does not affect
survival rate. Despite accurate resection, annual control
investigations should be offered to all patients harboring
SCTs, because late recurrence cannot be easily predicted
yet.
Keywords: Sacrococcygeal teratoma, immature terato-
ma, yolk sac tumor, local relapse, follow-up, histological
reevaluation.
Introduction
Sacrococcygeal teratoma (SCT) is the most frequent
congenital tumor occurring in 30–40,000 live births with
a female prevalence of 3 to 4 times [1–6]. At birth, more
than 90% of SCTs are “benign”, but up to 10% can show a
primarily malignant component [7–9]. Although these
experiences are worldwide known, the behavior of con-
genital teratomas remains poorly understood and is
frequently considered unpredictable, but studies of
large series with follow-up are very few [10, 11]. On one
hand, benign SCTs have a certain potential to malignant
manifestations increasing with age, i.e. at the age of 9
months in about 70% of cases of malignant SCTs [2, 3, 7,
9, 12]. On the other hand, malignant relapses of SCT after
primary resection classified as benign initially may de-
velop later on [2, 9, 13, 14]. Furthermore SCTs, depen-
dent on their position, size and dignity, can be
associated with intrauterine complications, such as uro-
logical, anorectal and osteomuscular ones, which can be
indistinct at birth [2, 7, 12, 14, 15]. Similar, but now
functional problems can occur after resection of SCTs
concerning the emptying of the bladder, defecation and/
or the function of the perineal region or/and the lower
extremities [7, 14, 16, 17].
Reevaluation of surgical procedures and histopath-
ologic diagnoses belongs to measures of quality control
Correspondence: Josef Hager, M.D., Department of Pediatric Sur-
gery, Medical University of Innsbruck, 6020 Innsbruck, Austria.
Fax: þþ43-50504-25693
E-mail: josef.hager@i-med.ac.at
SCT – a single center study of 43 years (1968–2011) © Springer-Verlag 4/2012 Eur Surg 255
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