Author(s)

Jinping Liu, Fei Zhai, Peng Ge, Jinhai Lu, Yi Qin, Xuguo Sun

Department of Medical Laboratory College, Tianjin Medical University, Tianjin, China.
Department of Neurology, Tianjin Medical University Hospital, Tianjin, China.

Objects: To investigate the pathogenesis of amyloid presented in uterine leiomyoma. Methods: 36 uterine leiomyoma patients were recruited and divided into two groups according to Congo red staining results. 6 cases are Congo red staining-positive, and 30 cases Congo red staining-negative which represented amyloid positive and amyloid negative respectively. All patients’ serum total protein (TP), albumin (Alb) and prealbumin (PA) levels were measured as well as blood hemoglobin (Hb), cell counts of white blood cell (WBC), neutrophils (NEU) and lymphocyte (LYM). Glycogen in tissue was compared between amyloid accumulated and amyloid negative sections with periodic acid schiff staining (PAS) in leiomyoma patients. Results: All of blood Hb concentration, WBC, NEU and LYM have not been found significant differences between two groups. Also no obvious infiltration of inflammatory cells was observed in tissue with amyloid deposition in uterine leiomyoma patients. And levels of TP, Alb and prealbumin have not been found significant differences between two groups. The amyloid was negative in leiomyoma entity cells range by Congo red staining, while small blood vessels in myoma tissues were positively detected with high rate. Amyloid was found in normal tissue around myoma as well as in blood vessel of pseudo-capsule. Increased PAS-positive material induced by leiomyoma was not correlated with amyloid deposition. Conclusions: Metabolic changes in the setting of functional alterations of cell in local microenvironment with uterine leiomyoma, may be related to the amyloid deposition.

Amyloid; Uterine Leiomyoma; Pathogenesis

Liu, J. , Zhai, F. , Ge, P. , Lu, J. , Qin, Y. and Sun, X. (2012) Investigation of amyloid deposition in uterine leiomyoma patients. Health, 4, 522-525. doi: 10.4236/health.2012.48083.