Javascript must be enabled to continue!
THE MYOMATOUS ERYTHROCYTOSIS SYNDROME
View through CrossRef
Uterine leiomyomas are the most common benign pelvic tumours in females.Rarely they are associated with symptoms of ectopic hormone production. One of thesesyndromes is the myomatous erythrocytosis syndrome, which is a triad of polycythaemia,fibroid(s) and resolution of the polycythaemia after hysterectomy. The case presented is of apost-menopausal lady found to have a Hb of 21 during workup of a pelvic mass. A diagnosis ofsecondary polycythemia due to ectopic erythropoietin production by the fibroid was made. Afterfive sessions of phlebotomiesa target Hb of 15 was obtained for surgery. The haematologicalvalues restored to normal three days post-operatively. It has been postulated that all fibroidsproduce erythropoietin. Recognition and proper management of this condition is importantto differentiate between primary and secondary polycythaemia as primary polycythemiais a thromboembolic condition, to avoid un-necessary investigations and to prevent anycomplications secondary polycythaemia may have per-operatively.
Independent Medical Trust
Title: THE MYOMATOUS ERYTHROCYTOSIS SYNDROME
Description:
Uterine leiomyomas are the most common benign pelvic tumours in females.
Rarely they are associated with symptoms of ectopic hormone production.
One of thesesyndromes is the myomatous erythrocytosis syndrome, which is a triad of polycythaemia,fibroid(s) and resolution of the polycythaemia after hysterectomy.
The case presented is of apost-menopausal lady found to have a Hb of 21 during workup of a pelvic mass.
A diagnosis ofsecondary polycythemia due to ectopic erythropoietin production by the fibroid was made.
Afterfive sessions of phlebotomiesa target Hb of 15 was obtained for surgery.
The haematologicalvalues restored to normal three days post-operatively.
It has been postulated that all fibroidsproduce erythropoietin.
Recognition and proper management of this condition is importantto differentiate between primary and secondary polycythaemia as primary polycythemiais a thromboembolic condition, to avoid un-necessary investigations and to prevent anycomplications secondary polycythaemia may have per-operatively.
Related Results
Diagnosis, Management, and Outcomes of Drug-Induced Erythrocytosis: A Systematic Review
Diagnosis, Management, and Outcomes of Drug-Induced Erythrocytosis: A Systematic Review
Background: Secondary erythrocytosis refers to an elevation in hemoglobin > 160 g/L in women or > 165 g/L in men that is not due to an underlying myeloproliferative n...
Diagnosis, management, and outcomes of drug-induced erythrocytosis: a systematic review
Diagnosis, management, and outcomes of drug-induced erythrocytosis: a systematic review
Abstract
Secondary erythrocytosis refers to an elevation in hemoglobin or hematocrit due to elevated serum erythropoietin levels. Medications including testostero...
Diagnosis and Treatment of Erythrocytosis
Diagnosis and Treatment of Erythrocytosis
An erythrocytosis arises when the red cell mass is increased. This can be due to a primary intrinsic defect in the erythroid progenitor cells or secondary to erythropoietin product...
Differential Diagnosis of Neurogenic Thoracic Outlet Syndrome: A Review
Differential Diagnosis of Neurogenic Thoracic Outlet Syndrome: A Review
Abstract
Thoracic outlet syndrome (TOS) is a complex and often overlooked condition caused by the compression of neurovascular structures as they pass through the thoracic outlet. ...
Three in One: Systemic Lupus Erythematosus, HELLP Syndrome, and Antiphospholipid Syndrome: A Case Report and Literature Review
Three in One: Systemic Lupus Erythematosus, HELLP Syndrome, and Antiphospholipid Syndrome: A Case Report and Literature Review
Abstract
Introduction
Systemic lupus erythematosus (SLE) is a multisystem autoimmune disease commonly affecting women of reproductive age. Its overlap with HELLP syndrome (Hemolysi...
TEMPI syndrome in a 57-year-old man: a case report
TEMPI syndrome in a 57-year-old man: a case report
Background:
The “TEMPI” syndrome consists of five distinct clinical features: telangiectasias (T), erythrocytosis with elevated erythropoietin (EPO) levels (E), monoclonal gammopat...
Secondary Erythrocytosis, a Predominant Cause of Polycythemia- Clinical and Laboratory Evaluation of Polycythemia in a Tertiary Care Center
Secondary Erythrocytosis, a Predominant Cause of Polycythemia- Clinical and Laboratory Evaluation of Polycythemia in a Tertiary Care Center
Aims: Polycythemia refers to an increased production of red blood cells from bone marrow. It is one of the frequent reasons for a hematology consultation. The present work aimed to...
Characteristics of acute ischemic stroke in hospitalized patients in Tibet: A retrospective comparative study
Characteristics of acute ischemic stroke in hospitalized patients in Tibet: A retrospective comparative study
Abstract
Background: Lots of studies of acute ischemic stroke (AIS) had been conducted at low altitude regions, and related findings were used to instruct clinic management...


