Rare case of blood sweating or hematohidrosis syndrome

Published On 2018-12-08 12:30 GMT   |   Update On 2018-12-08 12:30 GMT
A rare case of blood-sweating or hematohidrosis syndrome has appeared in Canadian Medical Association Journal. The case has been reported by Roberto Maglie at Department of Medical and Surgical Critical Care, Section of Dermatology, University of Florence, Florence, Italy and colleagues.

Hematohidrosis is an uncommon disease characterized by spontaneous discharge of “blood sweat” through intact skin. Various causes have been proposed, including systemic diseases, such as vicarious menses and coagulopathies (albeit historically reported in malaria, scurvy and epilepsy), exertion and psychogenic disorders, in which bleeding might be the result of exacerbated sympathetic nervous system activation.


A 21-year-old woman was admitted to a general medical ward with a three-year history of self-limited episodes of bleeding from her palms and face despite no evidence of skin lesions. There was no obvious trigger for the bleeding, which could occur while she was asleep and during times of physical activity. She stated that more intense bleeding occurred during times of perceived emotional stress. Episodes lasted from one to five minutes.


 

Courtesy CMAJ

The patient had become socially isolated owing to embarrassment over the bleeding and she reported symptoms consistent with major depressive disorder and panic disorder. There was no history of psychosis.

The differential diagnosis included factitious disorder and an uncommon condition known as hematohidrosis. Laboratory investigations including a complete blood count and coagulation studies (prothrombin time, activated partial thromboplastin time, fibrinogen and D-dimer) were normal. No evidence was found to support a diagnosis of a factitious disorder.

Her depression and anxiety disorder were treated with paroxetine and clonazepam, but her bleeding continued. During admission, it was observed that the discharge of blood-stained fluid from her face.

Based on the presence of erythrocytes on microscopic examination (excluding disorders that induce “coloured sweat” secretion, such as chromhidrosis and pseudochromhidrosis), she was diagnosed with hematohidrosis. Histologic analysis of the skin in an area of bleeding was normal.

This patient was treated with propranolol (20 mg/day), based on its use in similar cases in the literature, and this led to a marked reduction, although not a complete remission of her bleeding.

Learning Points:-
• Hematohidrosis is an uncommon disease characterized by spontaneous discharge of “blood sweat” through intact skin.

• Various causes have been proposed, including systemic diseases, such as vicarious menses and coagulopathies (albeit historically reported in malaria, scurvy and epilepsy), exertion and psychogenic disorders, in which bleeding might be the result of exacerbated sympathetic nervous system activation.

• In the literature, there is no single explanation of the source of bleeding in hematohidrosis. Despite the fluid’s sweat-like appearance, the hypothesis that blood passes through eccrine ducts, induced by abnormal constrictions and expansions of periglandular vessels, has not yet been proven.

• Bleeding has also reportedly occurred through areas without sweat glands or through the follicles, and the presence of dermal defects leading to blood-filled spaces exuding via follicular openings or directly into the skin surface has also been proposed.


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Article Source : Canadian Medical Association Journal

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