Diagnosis and Treatment > Signs and Symptoms
Search for other papers by Aishah Ekhzaimy in
Google Scholar
PubMed
Search for other papers by Afshan Masood in
Google Scholar
PubMed
Search for other papers by Seham Alzahrani in
Google Scholar
PubMed
Search for other papers by Waleed Al-Ghamdi in
Google Scholar
PubMed
Search for other papers by Daad Alotaibi in
Google Scholar
PubMed
Search for other papers by Muhammad Mujammami in
Google Scholar
PubMed
Summary
Central diabetes insipidus (CDI) and several endocrine disorders previously classified as idiopathic are now considered to be of an autoimmune etiology. Dermatomyositis (DM), a rare autoimmune condition characterized by inflammatory myopathy and skin rashes, is also known to affect the gastrointestinal, pulmonary, and rarely the cardiac systems and the joints. The association of CDI and DM is extremely rare. After an extensive literature search and to the best of our knowledge this is the first reported case in literature, we report the case of a 36-year-old male with a history of CDI, who presented to the hospital’s endocrine outpatient clinic for evaluation of a 3-week history of progressive facial rash accompanied by weakness and aching of the muscles.
Learning points:
-
Accurate biochemical diagnosis should always be followed by etiological investigation.
-
This clinical entity usually constitutes a therapeutic challenge, often requiring a multidisciplinary approach for optimal outcome.
-
Dermatomyositis is an important differential diagnosis in patients presenting with proximal muscle weakness.
-
Associated autoimmune conditions should be considered while evaluating patients with dermatomyositis.
-
Dermatomyositis can relapse at any stage, even following a very long period of remission.
-
Maintenance immunosuppressive therapy should be carefully considered in these patients.
Search for other papers by Natassia Rodrigo in
Google Scholar
PubMed
Search for other papers by Samantha Hocking in
Google Scholar
PubMed
Summary
This case illustrates the exceedingly rare phenomenon of transient diabetes insipidus, in association with pre-eclampsia, occurring in the post-partum period following an in vitro fertilisation pregnancy, in an otherwise well 48-year-old lady. Diabetes insipidus can manifest during pregnancy, induced by increased vasopressinase activity secreted by placental trophoblasts and usually manifests in the third trimester. This presentation elucidates not only the intricate balance between the physiology of pregnancy and hormonal homeostasis, but also the importance of post-partum care as the physiological changes of pregnancy still hold pathological potential in the weeks immediately following delivery.
Learning points:
-
Diabetes insipidus (DI) is a rare complication of pregnancy occurring in 1 in 30 000 pregnancies.
-
It is associated with excessive vasopressinase activity, secreted by placental trophoblasts, which increases the rate of degradation of anti-diuretic hormone.
-
It is responsive to synthetic desmopressin 1-deanimo-8-d-arginine vasopressin as this form is not degraded by placental vasopressinase.
-
Vasopressinase is proportional to placental weight, which is increased in pregnancies conceived with assisted reproductive techniques including in vitro fertilisation.
-
Vasopressinase-induced DI is associated with pre-eclampsia.