Calcium pyrophosphate dihydrate deposition disease in the temporomandibular joint: diagnosis and treatment
Background Calcium pyrophosphate dihydrate deposition disease (CPDD) is a rare disease in the temporomandibular joint (TMJ) space. It forms a calcified crystal mass and induces a limitation of joint movement. Case presentation The calcified mass in our case was occupied in the left TMJ area and exte...
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Published in | Maxillofacial plastic and reconstructive surgery Vol. 40; no. 1; pp. 19 - 6 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
Berlin/Heidelberg
Springer Berlin Heidelberg
03.08.2018
SpringerOpen 대한악안면성형재건외과학회 |
Subjects | |
Online Access | Get full text |
ISSN | 2288-8586 2288-8101 2288-8586 |
DOI | 10.1186/s40902-018-0158-0 |
Cover
Summary: | Background
Calcium pyrophosphate dihydrate deposition disease (CPDD) is a rare disease in the temporomandibular joint (TMJ) space. It forms a calcified crystal mass and induces a limitation of joint movement.
Case presentation
The calcified mass in our case was occupied in the left TMJ area and extended to the infratemporal and middle cranial fossa. For a complete excision of this mass, we performed a vertical ramus osteotomy and resected the mass around the mandibular condyle. The calcified mass in the infratemporal fossa was carefully excised, and the segmented mandible was anatomically repositioned. Scanning electronic microscopy (SEM)/energy-dispersive X-ray spectroscopy (EDS) microanalysis was performed to evaluate the calcified mass. The result of SEM/EDS showed that the crystal mass was completely composed of calcium pyrophosphate dihydrate. This result strongly suggested that the calcified mass was CPDD in the TMJ area.
Conclusions
CPDD in the TMJ is a rare disease and is difficult to differentially diagnose from other neoplasms. A histological examination and quantitative microanalysis are required to confirm the diagnosis. In our patient, CPDD in the TMJ was successfully removed via the extracorporeal approach. SEM/EDS microanalysis was used for the differential diagnosis. |
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Bibliography: | ObjectType-Case Study-2 SourceType-Scholarly Journals-1 ObjectType-Feature-4 content type line 23 ObjectType-Report-1 ObjectType-Article-3 https://jkamprs.springeropen.com/articles/10.1186/s40902-018-0158-0 |
ISSN: | 2288-8586 2288-8101 2288-8586 |
DOI: | 10.1186/s40902-018-0158-0 |