Case Reports in Obstetrics and Gynecology
Volume 2018 (2018), Article ID 6073204, 7 pages
https://doi.org/10.1155/2018/6073204

Case Report

Ultrasound Presentation of a Disseminated Fetal and Neonatal Rhabdoid Tumor

Yolaine Joueidi,¹ Aline Rousselin,¹ Céline Rozel,² Philippe Loget,³ Dominique Ranchere Vince,⁴ Sylvie Odent,5,6 Franck Bourdeaut,⁷ Vincent Lavoue,1,6 and Maela Le Lous¹

¹Department of Obstetrics and Gynaecology, CHU de Rennes, Hospital Anne de Bretagne, 16 Bd de Bulgarie, BP 90347, 35 203 Rennes Cedex 2, France
²Department of Radiology, CHU de Rennes, Hospital Anne de Bretagne, 16 Bd de Bulgarie, BP 90347, 35 203 Rennes Cedex 2, France
³Department of Pathology, CHU de Rennes, Hospital Pontchaillou, 2 rue Henri Le Guilloux, 35033 Rennes Cedex 9, France
⁴Department of Pathology, Leon Berard Center, 28 rue Laennec, 69008 Lyon, France
⁵Department of Genetics, CHU de Rennes, Hospital Anne de Bretagne, 16 Bd de Bulgarie, BP 90347, 35 203 Rennes Cedex 2, France
⁶Medical School, University of Rennes 1, 2 Avenue du Professeur Léon Bernard, 35000 Rennes, France
⁷Institut Curie, Paris Sciences et Lettres Research University, Inserm U830, Laboratoire de Genetique et Biologie des Cancers, 26 rue d’Ulm, 75005 Paris, France

Correspondence should be addressed to Yolaine Joueidi; yolaine.joueidi@orange.fr

Received 2 December 2017; Accepted 8 January 2018; Published 31 January 2018

Academic Editor: Erich Cosmi

Copyright © 2018 Yolaine Joueidi 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.

This is a case report of a disseminated fetal rhabdoid tumor discovered at 32 weeks of gestation in a 29-year-old woman on immunosuppressive therapy. The mother consulted for a decrease in fetal movement. Fetal ultrasound showed signs of a disseminated tumor affecting the left armpit, liver, spleen, and limbs. A caesarian section was performed because of signs of fetal distress. Immunohistochemical analysis of a fetal biopsy showed deletion of the SMARCB1 gene. Pathological analysis of the placenta showed a rhabdoid tumor invading both fetal and maternal compartments. The mother underwent a whole-body MRI, and no metastasis was found. To the best of our knowledge, this is the first report of a disseminated rhabdoid tumor invading both fetal and maternal compartments.

1. Case Report

A 29-year-old pregnant woman who was being treated with azathioprine for autoimmune hepatitis consulted at 32 weeks of gestation for decreased fetal movement. Obstetric ultrasound revealed many heterogeneous, hypervascular fetal tumors in the left armpit (Figure 1), intra-abdominal organs, and subcutaneous space (Figure 2). There was no sign of fetal cardiac insufficiency or anemia (no pericardial effusion and the middle cerebral artery peak systolic velocity was 50 cm/sec or 1,07 MoM).

Figure 1: Fetal ultrasound showing the tumor in the left armpit.

(a)

(b)

(c)

(d)

Figure 2: Other tumor sites on the iliac bone (a), intra-abdominal organs (b), left foot (c), and left thigh (d) found by ultrasound examination.

Fetal wellbeing was monitored daily and fetal lung maturity was induced at 32 weeks of gestation and 2 days with 12 mg of betamethasone repeated at 24 hours.

Two days later, a caesarian section was performed because of signs of fetal distress by fetal heart rate monitoring. The child presented immediately difficulties in adapting to extrauterine life and was cared for in the pediatric intensive care unit (Figure 3). First aid revealed that the child was anemic at birth (hemoglobin at 11,8 g/dl) with a pulmonary arterial hypertension on cardiac ultrasound. A body scan (Figure 4) and a biopsy of a cutaneous tumor were performed and showed characteristics of a rhabdoid tumor (small round nuclei, granular chromatin, and eosinophilic cytoplasm). The immunohistochemical analysis revealed a loss of SMARCB1 protein expression and pathological examination of the placenta showed an invasion of both fetal and maternal compartments (Figure 5). Because of prematurity, circulatory failure, and severe renal dysfunction with anuria, chemotherapy was contraindicated, and the decision was made with the parents to withdraw care. The child died at day 5 of multivisceral failure. The mother underwent a whole-body MRI to identify potential metastasis, but none was found.

Figure 3: Pediatric examination of the newborn.

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(b)

(c)

(d)

Figure 4: CT scan with a contrast agent showing the axillary mass compressing the chest (a) and numerous intra-abdominal tumors involving the liver, spleen, and right kidney (b, c, d) in axial, frontal, and sagittal views.

Figure 5: Pathological analysis of the placenta.

The INI1/SMARCB1 analysis conducted by Sanger sequencing of all exons and exon/intron boundaries and a Multiplex Ligation-dependent Probe Amplification (MLPA) to detect copy number alterations revealed a homozygous deletion of the 9 exons in tumor DNA. This alteration was not found in the child’s germ line nor in the parents. Therefore, the hypothesis of an inherited predisposition involving the SMARCB1 gene was excluded, and the hypothesis of a postzygotic (de novo) genetic alteration was retained.

2. Discussion

Fetal rhabdoid tumors are rare, aggressive, and often diagnosed at metastatic stage. They have a poor prognosis with a high mortality rate before one year of life. The average age at diagnosis is 11 months. These tumors are reported most frequently in the central nervous system, kidneys, and soft tissue. They are sometimes discovered in utero following severe anemia secondary to tumor rupture or on the presence of many disseminated nodules [1]. Only 6 other cases of prenatal diagnosis of fetal rhabdoid tumor are described in literature. Their localization, the ultrasound description, the gestational age at diagnosis, and the placental tumor invasion are reported in Table 1 [2–8]. These tumors affected both boys and girls. They were in all cases diagnosed during the third trimester and invaded the placenta in 3 cases. They were most often metastatic at time of diagnosis and the birth occurred shortly after the diagnosis in all the cases with a survival less than 15 days.

Table 1: Cases of prenatal diagnosis of rhabdoid tumor.

Author
Year
Localization
Ultrasound exam
Newborn sex
WG at diagnosis
WG at Birth
Genetics
Fetal part of the Placenta involved
Maternal
Part of the placenta involved
Child
survival

White et al.
1999
Case : face and neck, anterior cranial fossa, metastasis
NS
F
33
NS
abnormality of chr 22q11
Yes
NS
Few minutes

Ohyama et al.
2000
Liver and skin metastasis
NS
M
33
33
NS
Yes
Yes
4 days

Staehelin et al.
2000
Right shoulder and sacral tumor
Cystic and solid tumor + polyhydramnios
F
31
32
46 XX,
inv (p13p15)
No
No
6 days

Hösli et al.
2001

Leader et al.
2002
Neck and chest and left arm + metastasis
Vascularized tumor + polyhydramnios
F
29
30
47XX, +7/47
NS
NS
5 days

Fuchs et al.
2004
Left kidney
Homogeneous vascularized mass of left kidney + polyhydramnios
M
26
29
NS
Analysis refused by parents
Analysis refused by parents
4 hours

Kwon et al.
2009
Right arm
Solid tumor + polyhydramnios
M
35
35
NS
No
No
12 days

Joueidi et al.
2014
Left armpit + metastasis
Vascularized heterogeneous tumor + polyhydramnios
M
32
32
Mutation SMARCB1 del 22q11
Yes
Yes
5 days

F = female; M = male; WG: weeks of gestation; Chr: chromosome; NS: not specified.

The pathological diagnosis of rhabdoid tumor is based on characteristic cells with a round vesicular nucleus, a prominent nucleolus, and round or oval eosinophilic inclusion bodies. These cells show a deletion in chromosome 22q11 or mutations of the SMARCB1 gene, a tumor suppressor gene, by immunohistochemical analysis. The majority of rhabdoid tumors arise from somatic loss of both copies of SMARCB1, which affects the formation of chromatin remodeling complexes. SMARCB1 mutations can arise de novo or be secondary to a germline mutation, which should prompt genetic counseling [9]. In the 6 cases described in literature, 3 gave the genetic characteristics of the tumor but only one evoked an abnormality of chromosome 22q11.

Invasion of both fetal and maternal compartments of the placenta by tumor cells is extremely rare. In the literature, 36 cases of invasion of chorionic villi (fetal space) have been reported, but only 3 cases have been reported with invasion of the intervillous space with a risk of maternal dissemination of the tumor [10, 11] (Table 2). There have been no cases of maternal disease after complete examination, but this possibility should be explored in order to treat the mother as soon as possible, if necessary.

Table 2: Reported cases of placenta involvement by fetal malignancies.

Author
Fetal
malignancy
Weight live
Survival
Fetal part of the placenta involved
Maternal part  of the placenta involved
Kind of placenta involvement
Maternal disease
Maternal follow up

Ohyama et al. (2000)
Epithelial tumor of the liver with metastasis
1774 g
4 days
Yes
Yes
Chorionic villi and intervillous spaces
No maternal disease

De Tar and Biggerstaff (2006)
Renal rhabdoid tumor with metastasis
3130 g
Died during neonatal care
Yes
Yes
Chorionic villi and intervillous spaces
No maternal disease
2 years

Reif et al. (2014)
Soft tissue sarcoma of the left index finger
3000 g
4 months
Yes
Yes
Chorionic villi and intervillous spaces
No maternal disease
9 months

Joueidi et al. (2014)
Disseminated rhabdoid tumor
2645 g
5 days
Yes
Yes
Chorionic villi and intervillous spaces
No maternal disease
2 years

Azathioprine is a reported mutagen in vitro and in vivo in mice, but no case of human fetal malignancy has been reported in connection with maternal treatment [12].

Rhabdoid fetal tumors are aggressive with a difficult ultrasound diagnosis and a poor prognosis. The placenta should be analyzed for infiltration of the maternal side and tumor dissemination. Genetic counseling should be recommended for antenatal diagnosis of SMARCB1 mutation, and preimplantation screening may be discussed in cases of germline mutation.

Conflicts of Interest

The authors declare that there are no conflicts of interest regarding the publication of this paper.

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