Challenge in Diagnosing Osteopoikilosis: A Case Report

Authors

  • Yuni Artha Prabowo Putro Department of Orthopaedics and Traumatology, Faculty of Medicine, Public Health and Nursing, Universitas Gadjah Mada, Dr. Sardjito General Hospital, Yogyakarta, Indonesia image/svg+xml
  • Rahadyan Magetsari Department of Orthopaedics and Traumatology, Faculty of Medicine, Public Health and Nursing, Universitas Gadjah Mada, Dr. Sardjito General Hospital, Yogyakarta, Indonesia image/svg+xml
  • Morteza Bahesdhi Salipi Department of Orthopaedics and Traumatology, Faculty of Medicine, Public Health and Nursing, Universitas Gadjah Mada, Dr. Sardjito General Hospital, Yogyakarta, Indonesia image/svg+xml
  • A. Faiz Huwaidi Department of Orthopaedics and Traumatology, Faculty of Medicine, Public Health and Nursing, Universitas Gadjah Mada, Dr. Sardjito General Hospital, Yogyakarta, Indonesia https://orcid.org/0000-0001-9221-6826
  • Paramita Ayu Saraswati Department of Orthopaedics and Traumatology, Faculty of Medicine, Public Health and Nursing, Universitas Gadjah Mada, Dr. Sardjito General Hospital, Yogyakarta, Indonesia

DOI:

https://doi.org/10.3889/oamjms.2022.10889

Keywords:

Osteopoikilosis, Diagnosis, Rare bone disease

Abstract

Background: Osteopoikilosis is a rare benign osteosclerotic dysplasia and occurs in 1/50,000 people. Osteopoikilosis is inherited in an autosomal dominant and associated with several clinical manifestations. Currently, there is no agreement on diagnosing osteopoikilosis.  In this case report, we describe a 24-year-old female patient complaining of a lump and pain in the sole of the right foot. 

Case presentation: A 24 years female complained of a painful lump on the right pedis for one year. On physical examination of the right foot found a painful lump with firm boundaries, no sign of inflammation or trauma, and 1 cm x 0,5 cm x 0,5 cm in size. We perform a radiographic examination including bone survey and found multiple homogenous sclerotic lesions were spread over almost all visualized bony structures with oval to round in shape, varied in size, and well-defined borders. The laboratory examination shows normal results. Based on the findings described above, we diagnosed the patient with osteopoikilosis. The patient was provided with analgesics as therapy and periodic observation.

Conclusion: Osteopoikilosis is a rare case and is generally found incidentally on radiographic examination. The combination of history taking, clinical manifestations, and typical radiographic findings is sufficient to establish the diagnosis. This can prevent unnecessary examinations or invasive procedures.

Keywords: Osteopoikilosis, diagnosis, rare bone disease

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References

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Published

2022-02-05

How to Cite

1.
Putro YAP, Magetsari R, Salipi MB, Huwaidi AF, Saraswati PA. Challenge in Diagnosing Osteopoikilosis: A Case Report. Open Access Maced J Med Sci [Internet]. 2022 Feb. 5 [cited 2024 Nov. 21];10(C):1-4. Available from: https://oamjms.eu/index.php/mjms/article/view/10889

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Case Report in Surgery

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