A complex and often confusing nomenclature is currently used for relatively rare syndromes characterized by sudden onset of joint pain in the lower limbs, absence of trauma, bone marrow edema and its resolution, both confirmed by the MRI, as well as a self-limiting course. These include transient osteoporosis of the hip (TOH), of the knee (TOK), of the foot and ankle and transient bone marrow edema syndrome. Our purpose was to review the literature in order to substantiate the hypothesis that these apparently different conditions may be synthesized into a single disease entity, termed transient primary bone marrow edema syndrome (TPBMES). Of a total of 546 patients scrutinized, 342 had TOH, 105 had TOH of pregnancy, and 49, mainly females, showed transient foot-and-ankle osteoporosis. TPBMES occurred also with systemic osteoporosis or in a migratory pattern. The six proposed subsets of TPBMES have in common a MRI-based diagnosis and remission, as well as a self-limiting course. Thus, the hypothesis of a single disease entity is sustainable. We conclude that the education of the medical profession regarding this rare disease should expand. The causes of the prolonged symptoms seen in the systemic osteoporosis and migratory subsets warrant further studies. The efficiency of our suggested modality of management should be validated in a large cohort.
Published in | American Journal of Internal Medicine (Volume 7, Issue 2) |
DOI | 10.11648/j.ajim.20190702.11 |
Page(s) | 27-32 |
Creative Commons |
This is an Open Access article, distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution and reproduction in any medium or format, provided the original work is properly cited. |
Copyright |
Copyright © The Author(s), 2019. Published by Science Publishing Group |
Joint Pain, Bone Pain, Transient Bone Marrow Edema Syndrome, Systemic Osteoporosis, Migratory Osteoporosis, Bisphosphonates, Aledronate, Synthesis
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APA Style
Nissim Ohana, Dimitri Sheinis, Daniel Benharroch. (2019). Transient Primary Bone Marrow Edema Syndrome - A Synthesis. American Journal of Internal Medicine, 7(2), 27-32. https://doi.org/10.11648/j.ajim.20190702.11
ACS Style
Nissim Ohana; Dimitri Sheinis; Daniel Benharroch. Transient Primary Bone Marrow Edema Syndrome - A Synthesis. Am. J. Intern. Med. 2019, 7(2), 27-32. doi: 10.11648/j.ajim.20190702.11
AMA Style
Nissim Ohana, Dimitri Sheinis, Daniel Benharroch. Transient Primary Bone Marrow Edema Syndrome - A Synthesis. Am J Intern Med. 2019;7(2):27-32. doi: 10.11648/j.ajim.20190702.11
@article{10.11648/j.ajim.20190702.11, author = {Nissim Ohana and Dimitri Sheinis and Daniel Benharroch}, title = {Transient Primary Bone Marrow Edema Syndrome - A Synthesis}, journal = {American Journal of Internal Medicine}, volume = {7}, number = {2}, pages = {27-32}, doi = {10.11648/j.ajim.20190702.11}, url = {https://doi.org/10.11648/j.ajim.20190702.11}, eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.ajim.20190702.11}, abstract = {A complex and often confusing nomenclature is currently used for relatively rare syndromes characterized by sudden onset of joint pain in the lower limbs, absence of trauma, bone marrow edema and its resolution, both confirmed by the MRI, as well as a self-limiting course. These include transient osteoporosis of the hip (TOH), of the knee (TOK), of the foot and ankle and transient bone marrow edema syndrome. Our purpose was to review the literature in order to substantiate the hypothesis that these apparently different conditions may be synthesized into a single disease entity, termed transient primary bone marrow edema syndrome (TPBMES). Of a total of 546 patients scrutinized, 342 had TOH, 105 had TOH of pregnancy, and 49, mainly females, showed transient foot-and-ankle osteoporosis. TPBMES occurred also with systemic osteoporosis or in a migratory pattern. The six proposed subsets of TPBMES have in common a MRI-based diagnosis and remission, as well as a self-limiting course. Thus, the hypothesis of a single disease entity is sustainable. We conclude that the education of the medical profession regarding this rare disease should expand. The causes of the prolonged symptoms seen in the systemic osteoporosis and migratory subsets warrant further studies. The efficiency of our suggested modality of management should be validated in a large cohort.}, year = {2019} }
TY - JOUR T1 - Transient Primary Bone Marrow Edema Syndrome - A Synthesis AU - Nissim Ohana AU - Dimitri Sheinis AU - Daniel Benharroch Y1 - 2019/05/15 PY - 2019 N1 - https://doi.org/10.11648/j.ajim.20190702.11 DO - 10.11648/j.ajim.20190702.11 T2 - American Journal of Internal Medicine JF - American Journal of Internal Medicine JO - American Journal of Internal Medicine SP - 27 EP - 32 PB - Science Publishing Group SN - 2330-4324 UR - https://doi.org/10.11648/j.ajim.20190702.11 AB - A complex and often confusing nomenclature is currently used for relatively rare syndromes characterized by sudden onset of joint pain in the lower limbs, absence of trauma, bone marrow edema and its resolution, both confirmed by the MRI, as well as a self-limiting course. These include transient osteoporosis of the hip (TOH), of the knee (TOK), of the foot and ankle and transient bone marrow edema syndrome. Our purpose was to review the literature in order to substantiate the hypothesis that these apparently different conditions may be synthesized into a single disease entity, termed transient primary bone marrow edema syndrome (TPBMES). Of a total of 546 patients scrutinized, 342 had TOH, 105 had TOH of pregnancy, and 49, mainly females, showed transient foot-and-ankle osteoporosis. TPBMES occurred also with systemic osteoporosis or in a migratory pattern. The six proposed subsets of TPBMES have in common a MRI-based diagnosis and remission, as well as a self-limiting course. Thus, the hypothesis of a single disease entity is sustainable. We conclude that the education of the medical profession regarding this rare disease should expand. The causes of the prolonged symptoms seen in the systemic osteoporosis and migratory subsets warrant further studies. The efficiency of our suggested modality of management should be validated in a large cohort. VL - 7 IS - 2 ER -