Primary acalvaria: a case report

Abstracts

Acalvaria é uma malformação congênita rara de patogênese desconhecida, na qual os ossos da abóbada craniana, a dura-máter e a musculatura associada estão ausentes, mas o sistema nervoso central costuma estar preservado. A teoria fisiopatogênica mais aceita sugere um defeito pós-neurulação, com disposição normal do ectoderma embrionário. O objetivo deste relato é descrever os achados de imagem neonatais da acalvaria primária.

Acalvaria primária; Defeito do crânio; Malformação congênita

CASE REPORTS

Primary acalvaria: a case report^*

Lívia Teresa Moreira Rios^I; Marília da Glória Martins^II; Vanda Maria Ferreira Simões^III; Marynéa do Vale Nunes^IV; Patrícia Franco Marques^V; Silvia Helena Cavalcante de Souza Godoy^VI

^IMaster, Coordinator at Unit of Imaging Diagnosis of the Service of Obstetrics and Gynecology, Hospital Universitário da Universidade Federal do Maranhão (HU-UFMA), São Luís, MA, Brazil

^IIPhD, Head of the Service of Obstetrics and Gynecology, Hospital Universitário da Universidade Federal do Maranhão (HU-UFMA), São Luís, MA, Brazil

^IIIPhD, Head of the Service of Neonatology, Hospital Universitário da Universidade Federal do Maranhão (HU-UFMA), São Luís, MA, Brazil

^IVMD, Specialist, Coordinator of the Neonatal ICU, Service of Neonatology, Hospital Universitário da Universidade Federal do Maranhão (HU-UFMA), São Luís, MA, Brazil

^VMD, Specialist at the Neonatal ICU, Service of Neonatology, Hospital Universitário da Universidade Federal do Maranhão (HU-UFMA), São Luís, MA, Brazil

^VIFellow Master degree, MD, Neonatal ICU, Service of Neonatology, Hospital Universitário da Universidade Federal do Maranhão (HU-UFMA), São Luís, MA, Brazil

Mailing address

ABSTRACT

Acalvaria is a rare congenital malformation of unknown pathogenesis characterized by the absence of the flat bones of the cranial vault, dura mater and associated muscles, while the central nervous system is usually preserved. The most accepted physiopathogenic theory suggests the presence of a postneurulation defect with normal placement the embryonic ectoderm. The present report describes neonatal imaging findings of primary acalvaria.

Keywords: Primary acalvaria; Skull defect; Congenital malformation.

INTRODUCTION

Acalvaria is a rare congenital malformation of unknown pathogenesis characterized by the absence of the flat bones of the cranial vault, dura mater and associated muscles, whit normal skull base and facial bones. The brain tissue is usually preserved although in some cases it may be abnormally developed^(1-4). This abnormality has been described as a fatal condition and is scarcely described in the literature⁽⁵⁾.

The present case report describes imaging findings of primary acalvaria characterized by the absence of the flat bones of the cranial vault.

CASE REPORT

A 15-year-old primigravida at 38 weeks' gestation was referred to the authors' institution for specialized prenatal follow-up. Previous ultrasonography performed at the 31st gestational week had identified fetal unilateral hydrocephalus. There was no maternal history of teratogenic medication, recent infection, diabetes mellitus, hypertension or exposure to drugs during the current pregnancy. Cesarean section was indicated. A female neonate was born at term weighting 2815 grams.

At clinical examination, the neonate's face was apparently normal, with presence of skin on the frontal region. Cerebral hemispheres prominence and a large defect of the cranial vault were the most obvious findings. The abnormality was characterized by the partial absence of the scalp and o the flat bones of the cranial vault, with a thin membranous layer overlying the brain tissue from which one could observe leakage of cephalorachidian fluid compatible with the pia mater (Figure 1). Frontal and parietal bones could not be palpated. The newborn was referred to the neonatal intensive-care unit where the investigation was pursued.

Immediately after birth, skull radiography demonstrated absence of frontal, parietal and temporal bones, and presence of facial and occipital bones (Figure 2). The findings were confirmed by computed tomography that also demonstrated unilateral ventricular dilatation (Figure 3). Abdominal ultrasonography and echocardiography did not demonstrate any abnormality.

The brain remained covered by the pia mater for five days. As a result of the growth process, at the sixth day of life, the brain tissue started breaking-up the thin membrane, becoming completely exposed at the tenth day of life. An attempt to close the bone defect was made with a bovine pericardium patch at the 12th day of life. The reconstruction progressed with a local infectious process and partial suture dehiscence.

After two months of life, signs of hypoxic ischemic neurological deterioration could already be observed. After four months of life, transfontanel ultrasonography demonstrated the presence of cystic areas in the brain resulting from hypoxicischemic vascular lesion (Figure 4). The neonate progressed to death at the fifth month of life because of respiratory and infectious complications.

DISCUSSION

Primary acalvaria is a rare congenital malformation characterized by either complete or partial absence of the flat bones of the cranial vault, dura mater and associated muscles, with normal skull base and facial bones. Usually, the defect is covered by skin. The intracranial contents are generally complete, although some abnormalities may be associated^(1-7).

The etiology and pathogenesis of such abnormality still remain unknown. During the embryonic development, after the anterior neuropore closure around the fourth week migration of the membranous neurocranium occurs under the ectoderm.

The condition is said secondary in cases where it is a result of amniotic band syndrome, neural tube defects or use of angiotensin-converting enzyme inhibitors during pregnancy. It is named hypocalvaria in the presence of hypoplastic cranial bones⁽⁶⁾.

Association with other malformations such as holoprosencephaly, hydrocephalus and micropolygyria, besides other facial, cardiac anomalies, omphaloceles, among others, may be observed^(1,6). The rare reports found in the literature suggest a predilection for female fetuses with normal karyotype⁽⁷⁾, in agreement with the description of the present case.

Presence of skin covering the cranial vault and partial scalp absence were observed. The presence of ectoderm-derived skin and scalp and the absence of cranial vault, dura mater and associated muscle as a result of mesenchymal migration characterize primary acalvaria.

In this case, association with an extensive type of aplasia cutis congenita cannot be ruled out. This disorder is characterized by the absence of a portion of skin; most of times (84%) manifesting as a defect on the scalp. The skull is affected in 14% to 30% of cases. Extensive and deep lesions are extremely rare, with a high mortality rate, and may involve the periosteum, the skull and the dura mater⁽⁸⁾.

REFERENCES

• 1. Harris CP, Townsend JJ, Carey JC. Acalvaria: a unique congenital anomaly. Am J Med Genet. 1993;46:694-9.
• 2. Raines C. Primary acalvaria. JDMS. 2006;22: 407-10.
• 3. Bianca S, Ingegnosi C, Auditore S, et al. Prenatal and postnatal findings of acrania. Arch Gynecol Obstet. 2005;271:256-8.
• 4. Khadilkar VV, Khadilkar AV, Nimbalkar AA, et al. Acalvaria. Indian Pediatr. 2004;41:618-20.
• 5. Evans C, Marton T, Rutter S, et al. Cranial vault defects: the description of three cases that illustrate a spectrum of anomalies. Pediatr Dev Pathol. 2009;12:96-102.
• 6. Barr M, Cohen MM Jr. ACE inhibitor fetopathy and hypocalvaria. The kiney-skull connection. Teratology. 1991;44:485-95.
• 7. Raupp P, Nork M, Kappel I. Primary acalvaria in a term newborn. J Pediatr. 2002;141:593.
• 8. Yang JY, Yang WG. Large scalp and skull defect in aplasia cutis congenita. Br J Plast Surg. 2000; 53:619-22.

*

Trabalho realizado na Universidade Federal do Maranhão (UFMA), São Luís, MA, Brasil.

Publication Dates

• Publication in this collection
  16 Sept 2010
• Date of issue
  Aug 2010

History

• Received
  17 Apr 2010
• Accepted
  24 May 2010