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Progressive Pseudorheumatoid Dysplasia or JIA?

1. Introduction

Spondyloepiphyseal dysplasia tarda with progressive arthropathy (SEDT-PA) is a rare hereditary disorder with autosomal recessive inheritance [1]. This primarily affects the articular cartilage [2].

It is characterized by short trunk and extremities, platyspondyly, kyphoscoliosis, coxa vara, genu valgum/varum, and abnormal shape and structure of the epiphyses of hand bones.

With time, this leads to disproportionate dwarfism with progressive involvement of the spine and epiphysis of long bones. Boys are affected more often [3, 4].

Since joint involvement in SEDT-PA may be confused with juvenile idiopathic arthritis (JIA), SEDT-PA is also called progressive pseudorheumatoid dysplasia of childhood (PPD) [5, 6].

It is a rare disorder with a global prevalence of only 1/1 000 000 with two-thirds of reported cases from Arabia [7].

2. Patient Information and Clinical Findings

The patient was an intelligent 10-year-old boy born at term after a normal pregnancy and delivery. His parents were not consanguineous and did not have any family history of joint problems although both parents had Arabic origins.

His birth weight, neonatal history, and developmental milestones were normal. His symptoms had started at the age of 7 years with pain in the right hip with limping. This was followed by pain in left hip with swelling and deformities in the hands, wrists, and elbows.

His condition was misdiagnosed by several medical practitioners and was treated as JIA with nonsteroidal anti-inflammatory medications. However, luckily the patient was not started on disease modifying antirheumatic drugs. His height on presentation was <3rd percentile and upper- to lower-body segment ratio was 0.83. On examination his hands showed bulky proximal and distal interphalangeal joints without any synovitis. There was mild fixed flexion deformity of fingers. Neurological examination was uneventful.

3. Diagnostic Assessment

Radiological examination showed platyspondyly with anterior beaking of vertebral bodies (Figure 1), irregular enlarged femoral epiphyses with narrowing of the hip joint spaces, premature osteoarthritis, and short femoral necks (Figure 2).

The phalangeal epiphyses and metaphyses were enlarged and osteoarthritic changes were present in the interphalangeal joints (Figure 3). Enlarged os trigonum was seen in foot X-rays (Figure 4).

Hematological investigations including serum calcium/ phosphate, thyroid hormones, full blood count, C reactive protein, erythrocyte sedimentation rate, rheumatoid factor, and antinuclear antibody levels were all negative. Mucopolysaccharides were negative in the urine with normal skull imaging.

4. Therapeutic Intervention and Follow-Up

The child was clinically having short stature with kyphoscoliosis, pigeon chest, and joint problems. X-ray images of the pelvis show irregular ossification of the heads and greater trochanters of the femora and the X-rays of spine showed generalized platyspondyly with anterior beaking. Considering these facts, differential diagnosis like Faber's disease, Morquio syndrome, Scheuermann's disease, and JIA should be ruled out.

A diagnosis of SEDT-PA was made with patients history, examination, and X-ray findings and the condition was explained to the family. Patient was treated with physiotherapy and was referred to the orthopedic surgeon for assessment and follow-up as he would need corrective surgery in future. Ophthalmological opinion was taken to exclude any eye involvement. Family was referred for genetic counseling.

Physiotherapy was arranged and patient was prescribed nonsteroidal anti-inflammatory medications to take when needed for joint pains.

5. Discussion

PPD disease generally begins between the ages of 2 and 8 years with abnormal gait and fatigability [8]. The differentiation between JIA and SEDT-PA is challenging and most cases are misdiagnosed in the beginning as JIA. However, the absence of laboratory changes indicating systemic or synovial inflammation and the presence of characteristic X-ray changes of spondyloepiphyseal dysplasia help in the differential diagnosis of SEDT-PA from JIA [9].

The main reasons for misdiagnosis appear to be onset in childhood with swelling and restriction of peripheral and axial joints and the rarity of the disease.

The main clinical features in PPD are arthralgia, joint contractures, enlarged metacarpophalangeal and interphalangeal joints, and short stature [10]. Reported associations include corneal changes and osteoporosis [11, 12]. Characteristic imaging findings will be generalized platyspondyly and epiphyseal involvement, with enlargement of both ends of the short tubular bones of the hands [13].

Although radiologic examination has high accuracy in the diagnosis of PPD, the definitive diagnosis is established with identification of the characteristic radiological findings and biallelic pathogenic variants in WISP3 on molecular genetic testing [14].

Treatment is mainly conservative. Physical therapy may help preserve joint mobility. Immobilization (e.g., casting) should be avoided. Total replacement arthroplasty of the hips for secondary degenerative changes may be required at an early age and genetic studies need to be done for family counseling.

6. Conclusion

Genetic musculoskeletal disorders should be remembered among childhood rheumatic problems so that inappropriate therapy can be prevented while appropriate therapy could be started on time and genetic counseling can be offered to the family for the next generations.

PPD:     Progressive pseudorheumatoid dysplasia
SEDT-PA: Spondyloepiphyseal dysplasia tarda with
         progressive arthropathy.


Written informed consent was obtained from the patients' guardians for the publication and use of images and investigation results in the present case report.

Competing Interests

The author has no competing interests.

Authors' Contributions

The author conducted the literature review and drafted and reviewed the manuscript.


The author is grateful to the patients' parents for their consent to include images in the present case report.


[1] R. Scuccimarri, E. M. Azouz, K. N. W. Duffy, F. Fassier, and C. M. Duffy, "Inflammatory arthritis in children with osteochondrodysplasias," Annals of the Rheumatic Diseases, vol. 59, no. 11, pp. 864-869, 2000.

[2] O. Cogulu, F. Ozkinay, C. Ozkinay, G. Sapmaz, O. Yalman, and H. B. Deveci, "Progressive pseudorheumatoid arthropathy of childhood," Indian Journal of Pediatrics, vol. 66, no. 3, pp. 455-460, 1999.

[3] M. L. Lateur, J. H. Klippel, and P. A. Dieppe, "Bone and joint dysplasias," in Rheumatology, vol. 7, pp. 1-10, Mosby-Year Book Europe, London, UK, 1994.

[4] W. H. Mc Alister, D. Resnick, and G. Niwayama, "Osteochondrodysplasias and other skeletal dysplasias," in Diagnosis of Bone and Joint Disorders, pp. 3442-3515,W.B. Saunders, Philadelphia, Pa, USA, 1988.

[5] S. Sarioglu, T. Arasil, A. Kucukdeveci, and Y. Gursel, "Spondyloepiphesael dysplasia tarda: a case report," T Klin J PM&R, vol. 3, pp. 93-96, 2003.

[6] S. Arslanoglu, H. Murat, and G. Ferah, "Spondyloepiphyseal dysplasia tarda with progressive arthropathy: an important form of osteodysplasia in the differential diagnosis of juvenile rheumatoid arthritis," Pediatrics International, vol. 42, no. 5, pp. 561-563, 2000.

[7] H. E. El-Shanti, H. Z. Omari, and H. I. Qubain, "Progressive pseudorheumatoid dysplasia: report of a family and review," Journal of Medical Genetics, vol. 34, no. 7, pp. 559-563, 1997.

[8] A. S. Teebi and S. A. Al Awadi, "Spondyloepiphyseal dysplasia tarda with progressive arthropathy: a rare disorder frequently diagnosed among Arabs," Journal of medical genetics, vol. 23, no. 2, pp. 189-191, 1986.

[9] S. Bal, H. Kocyigit, Y. Turan et al., "Spondyloepiphyseal dysplasia tarda: four cases from two families," Rheumatology International, vol. 29, no. 6, pp. 699-702, 2009.

[10] A. Cefle, K. Cefle, M. Tunaci, S. Ozturk, and S. Palanduz, "A case of progressive pseudorheumatoid arthropathy of 'childhood' with the diagnosis delayed to the fifth decade," International Journal of Clinical Practice, vol. 60, no. 10, pp. 1306-1309, 2006.

[11] S. Kurtulmus, K. B. Bayram, H. Kocyigit, S. Koksal-Avci, Y. Dincer-Turan, and A. Gurgan, "Spondyloepiphyseal dysplasia tarda and osteoporosis: a case report," Osteoporoz Dunyasindan, vol. 12, pp. 18-21, 2006.

[12] I. Batmaz, M. A. Sariyildiz, B. DIlek et al., "A case of spondyloepiphyseal dysplasia tarda coexisting with osteoporosis and mimicking spondyloarthropathy," Turkiye Fiziksel Tip ve Rehabilitasyon Dergisi, vol. 59, no. 3, pp. 260-263, 2013.

[13] H. Kocyigit, R. Arkun, F. Ozkinay, O. Cogulu, N. Hizli, and A. Memis, "Spondyloepiphyseal dysplasia tarda with progressive arthropathy," Clinical Rheumatology, vol. 19, no. 3, pp. 238-241, 2000.

[14] G. S. Bhavani, H. Shah, A. B. Dalal et al., "Progressive pseudorheumatoid dysplasia," in GeneReviews at GeneTests Medical Genetics Information Resource, University of Washington, Seattle, Wash, USA, 1993-2016,

Geetha Wickrematilake

District General Hospital, Nuwara Eliya, Sri Lanka

Correspondence should be addressed to Geetha Wickrematilake;

Received 26 November 2016; Revised 15 January 2017; Accepted 5 February 2017; Published 21 February 2017

Academic Editor: Tamas Constantin

Caption: Figure 1: Platyspondyly with and anterior end plate abnormalities with defective ossification and anterior beaking of vertebral bodies.

Caption: Figure 2: Anteroposterior X-ray of the pelvis showing flattened and enlarged epiphyses of the femoral heads.

Caption: Figure 3: X-ray of hands showing epiphyseal enlargement of the metacarpophalangeal and interphalangeal joints with juxtaarticular osteopenia.

Caption: Figure 4: Lateral radiograph of right foot indicating mega os trigonum.
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Title Annotation:Case Report; juvenile idiopathic arthritis
Author:Wickrematilake, Geetha
Publication:Case Reports in Rheumatology
Article Type:Clinical report
Date:Jan 1, 2017
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