• Users Online: 111
  • Print this page
  • Email this page


 
 
Table of Contents
CASE REPORT
Year : 2017  |  Volume : 6  |  Issue : 5  |  Page : 238-240

A case report of prenatally detected achondrogenesis type II with an occipital cephalocele


1 Department of Radiology, Women Hospital, Tehran University of Medical Sciences, Tehran, Iran
2 Department of Obstetrics and Gynecology, Women Hospital, Tehran University of Medical Sciences, Tehran, Iran
3 Department of Radiology, Amiralam Hospital, Tehran University of Medical Sciences, Tehran, Iran
4 Rastaak Sonography Center, Tehran, Iran

Date of Submission18-Jun-2017
Date of Decision10-Jul-2017
Date of Acceptance01-Aug-2017
Date of Web Publication10-Oct-2017

Correspondence Address:
Mohamad Ali Kazemi
Department of Radiology, Amiralam Hospital, Sadi Street, Tehran
Iran
Login to access the Email id

Source of Support: None, Conflict of Interest: None


DOI: 10.4103/2305-0500.215936

Rights and Permissions
  Abstract 


Achondrogenesis is a very rare lethal skeletal disorder. Here we describe a case of prenatally diagnosed achondrogenesis type II in a 28 year-old woman at (17+4) wk. She had history of 5 first trimester missed abortions. The couple is consanguineous. Ultrasonography showed extreme micromelia, short neck and trunk, large head and prominent abdomen. Delayed ossification in sacral bones was detected and ossification of pubic rami was poor. There were associated large cystic hygroma, anasarca and also high occipital cephalocele. Posterior fossa was normal. Mild hypothelorism, depressed nasal bridge, low set ear and mild retrognathia were identified too. Amniocentesis result was compatible with a normal female fetus. Post mortem whole body radiography confirmed the diagnosis. To our knowledge, this is the second case report with association of cephalocele and achondrogenesis type II.

Keywords: Achondrogenesis type II, Cephalocele, Cystic hygroma, Lethal skeletal dysplasia


How to cite this article:
Moradi B, Adabi K, Kazemi MA, Masrour FF. A case report of prenatally detected achondrogenesis type II with an occipital cephalocele. Asian Pac J Reprod 2017;6:238-40

How to cite this URL:
Moradi B, Adabi K, Kazemi MA, Masrour FF. A case report of prenatally detected achondrogenesis type II with an occipital cephalocele. Asian Pac J Reprod [serial online] 2017 [cited 2020 Jul 12];6:238-40. Available from: http://www.apjr.net/text.asp?2017/6/5/238/215936




  1. Introduction Top


Achondrogenesis is one of lethal type of skeletal dysplasia, which is the most severe form with extreme micromelia[1]. It is characterized by short trunk, protuberant abdomen, disproportionatly large cranium and some degree of endochondral ossification deficiency[2]. Hydrops fetalis and some facial features as retrognathia also have been reported as associated abnormalities. They are divided into two groups, type I (A and B) and type II mainly based on radiological and clinical studies such as rib fractures and pattern of poorly ossified bones[3]. Type II is also called Langer-Saldino Achondrogenesis.

We report a case of type II achondrogenesis with occipital cephalocele in an 18 wk fetus diagnosed on prenatal sonography and post mortem radiography.


  2. Case report Top


A 28 years old gravida 6 para 0 at (17+4) wk was referred to our hospital with diagnosis of hydrops fetalis and tetra phocomelia. She had history of 5 first trimester missed abortions around 6-8 wk. The couple is first degree relative consanguineous without family history of skeletal abnormalities, teratogen exposure or any other disease.

Prenatal sonography at out center revealed, extreme micromelia (femur length: 4.4 mm, humerus length: 5 mm, tibia: 3.3 mm and ulna: 4.3 mm). Foot length (19 mm) was normal for fetal age and Femur length (FL)/foot ratio (0.23) was severely decreased. FL/ abdominal circumference ratio (0.02) was also severely decreased, in favor of lethal skeletal dysplasia. There was evidence of associated bell shaped and narrow thorax, short neck and trunk, prominent abdomen [enlarged abdominal circumference: 156 mm, (20+6) wk] and macrocephaly [head circumference: 162 mm, (19+1) wk]. Delayed ossification in sacral bones was detected and ossification of pubic rami were poor [Figure 1]A and [Figure 1]B. The ossification of skull and ribs appeared normal and there was no evidence of rib or other bone fracture. There was evidence of cystic hygroma and hydrops fetalis (extensive skin edema and mild plural effusion). In the evaluation of head and neck, a high occipital meningocele, mild hypothelorism, depressed nasal bridge, low set ear and mild retrognathia were evident [Figure 1]C.
Figure 1: Ultrasonography at (17+4) wk.
(A) Extreme micromelia (short arrow), bell shaped thorax (long arrow), prominent abdomen and cystic hygroma (wide arrow); (B) Delayed ossification of sacral bones (arrow); (C) Good ossification off skull and occipital cephalocele (arrow).


Click here to view


This study was approved by the local committee for ethics in research and permission to carry out the study was obtained from the parents and the informed consent was taken from them. Amniocentesis was compatible with normal 46 xx karyotype. Based on the mentioned findings, achondrogenesis type II was suggested. Parents chose termination of pregnancy and post mortem photography and babygram confirmed the diagnosis [Figure 2]. The size of fetus in [Figure 2] is 105 mm. In babygram extremely short limbs, narrow thorax with short ribs, short trunk, delayed ossification in sacrum, poor ossification of pubic bones and macrocephaly were evident. There was no bony fracture.
Figure 2: Post mortem baby gram showing delayed ossification of sacral bones, short trunk, macrocephaly and extremely short long bones.

Click here to view



  3. Discussion Top


Achondrogenesis is an osteochondysplasia that affects the growing cartilages and is caused by mutations in collagen genes.

It includes that a heterogeneous group of skeletal dysplasia which severely affect long bones length and is classified into type I and II[1],[3]. Inheritance of type I (Parenti – Franccaro) is autosomal recessive and characterized by poor ossification of the skull, pelvis and spine with rib fractures[1],[3]. Type II (Longer – Saldino) is usually caused by new autosomal dominant mutations in COL 2A1 gene. Type II is characterized by normal appearance of calvarium, absence of rib fracture and deficient ossification of spine (especially cervical and sacrum)[3],[4],[5]. Polyhydramnios and hydropic feature are also common as our case[1],[3]. Pattern of deficient ossification and presence of rib fracture are good clues in differentiating between type I and II. Normal appearing calvarium and absence of rib fracture are in favor of type II and vice versa[1]. Achondrogenesis can be differentiated from other lethal type skeletal dysplasia based on its features. In thanatophoric dysplasia, there is no deficient mineralization. The limbs are longer, and the thorax is narrow but is elongated in shape. Osteogenesis imperfecta is characterized by poor mineralization in multiple bones and multiple fractures are nearly hallmark of this dysplasia. Limbs are not as short as anchondrogenesis and head is not disproportionately large. Hypophosphatasia is characterized by diffuse hypo mineralization involving nearly all bones except clavicle. Micromelia is less severe comparing to achodrogenesis and there is no macrocrania[1],[3].

Nearly all differentiating features and prognostic appearances can be evaluated by detailed anomaly scan by an expert, and radiography is nearly pathognomonic confirming option. In less severe and challenging cases, histopathology and gene study are helpful[1],[4]. In our case, a high occiput cephalocele was present, and to the best of our knowledge, this is the second case with association of cephalocele and achondrogenesis type II[6]. Lethality can be evaluated based on literature by thorax abdominal circumference ratio of <0.6 or FL to abdominal circumference <0.16 (which is severely affected in our case) in the presence of hydrops feralis[7]. Long bones were extremely short in our case, which were hardly visible (FL/foot: 0.02) and caused misdiagnosis of tetra phocomelia in other center.

In conclusion, we have described a case of achondrogenesis type II with extreme micromelia, high occipital cephalocele, cystic hygroma and hydrops. Prenatal ultrasonography combined with post mortem radiography helped to reach the diagnosis.

Conflict of interest statement

The authors declare that they have no conflict of interest.



 
  References Top

1.
Faivre L, Cormier-Daire V. Achondrogenesis. Orphanet encyclopedia; 2003.  Back to cited text no. 1
    
2.
Kodandapani S, Ramkumar V. Antenatal diagnosis of achondrogenesis type II. JNMA J Nepal Med Assoc 2009; 48(174): 155-157.  Back to cited text no. 2
    
3.
Taner MZ, Kurdoglu M, Taskiran C, Onan MA, Gunaydin G, Himmetoglu O. Prenatal diagnosis of achondrogenesis type I : A case report. Cases J 2008; 1(1): 406.  Back to cited text no. 3
    
4.
Forzano F, Lituania M, Viassolo A, Superti-Furga V, Wildhardt G, Zabel B, et al. A familial case of achondrogenesis type II caused by a dominant COL 2A1 mutation and “patchy” expression in the mosaic father. Am J Med Genet A 2007; 143A(23): 2815-2820.  Back to cited text no. 4
    
5.
Thomas D, Lejeune R, Mortier G, Duprez L, Puttemans T, Lamy C. Achondrogenesis, type II. Sonoworld 2003; 1: 14-15.  Back to cited text no. 5
    
6.
Fong K, Bedford M, Toi A. Ultrasound diagnosis of achondrogenesis type II with an occipital encephalocele at 15 weeks gestation. Ultrasound Obstet Gynecol 2015; 46: 122-184.  Back to cited text no. 6
    
7.
Nelson DB, Dashe JS, McIntire DD, Twickler DM. Fetal skeletal dysplasias, sonographic indices associated with adverse outcomes. J Ultrasound Med 2014; 33(6): 1085-1090.  Back to cited text no. 7
    


    Figures

  [Figure 1], [Figure 2]



 

Top
 
  Search
 
    Similar in PUBMED
   Search Pubmed for
   Search in Google Scholar for
 Related articles
    Access Statistics
    Email Alert *
    Add to My List *
* Registration required (free)  

 
  In this article
Abstract
1. Introduction
2. Case report
3. Discussion
References
Article Figures

 Article Access Statistics
    Viewed1371    
    Printed63    
    Emailed0    
    PDF Downloaded120    
    Comments [Add]    

Recommend this journal