Imaging Appearances in a Case of Tumoral Calcinosis
Tumoral calcinosis is an uncommon entity characterised by calcified para-articular masses as demonstrated most often on radiographs. It can occur at any age and is inherited as an autosomal dominant mode that has a variable clinical expression. Its biochemical hallmarks are hyperphosphataemia w...
Main Authors: | , |
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Format: | Article |
Language: | English |
Published: |
JCDR Research and Publications Pvt. Ltd.
2016-04-01
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Series: | International Journal of Anatomy Radiology and Surgery |
Subjects: | |
Online Access: | http://www.ijars.net/articles/PDF/2130/11-4487_F(P)_PF1(Vsu_Om)_PFA(Om)_PF2(PVSU).pdf |
Summary: | Tumoral calcinosis is an uncommon entity characterised
by calcified para-articular masses as demonstrated
most often on radiographs. It can occur at any age and
is inherited as an autosomal dominant mode that has a
variable clinical expression. Its biochemical hallmarks are
hyperphosphataemia with normocalcaemia and normal
renal function.
It is only rarely that one comes across a disease which is
so obvious in its clinical manifestations that it should easily be recognized and yet which is frequently misdiagnosed
and dismissed as something else for example “foreign body
reactions”, “old trauma”, “sebaceous cysts with secondary
calcification”, “periarticular giant cell tumours” and “unknown embryonic tumours” to quote a few examples. As
it has a potential to produce tumours weighing as much as
4,000 g, which are often multiple and cause pressure symptoms, which may necrose, recur after removal, cause considerable pain and morbidity and, may even endanger the of
the patient, it is entitled to a little more “respect”.
Unfamiliarity with tumoral calcinosis as well as the disease
processes that mimic this condition; impedes the correct
diagnosis thereby delaying the treatment, and an undue
alarm could be raised, possibly leading to unwarranted
surgical procedures. Hence, we all need to be familiar
with this entity. |
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ISSN: | 2277-8543 2455-6874 |