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S&M Cystadenoma, H Mole

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POLYCYSTIC OVARIES

 Polycystic ovarian disease (PCOD; formerly


termed SteinLeventhal syndrome) affects 3% to
6% ofreproductive-age women. The central
pathologic abnormality is numerous cystic
follicles or folliclecysts, often associated with
oligomenorrhea. Women with PCOD have
persistent anovulation, obesity (40%), hirsutism
(50%).
SEROUS CYSTADENOMA
 MOST COMMON NEOPLASMS OF OVARY
 CAN BE FOUND AT ANY AGE
 MC BETWEEN 20-50 YRS OF AGE
 BILATERAL INVOLVEMENT OCCUR IN 20%
CASES
GROSS
 IT IS UNILOCULAR, THIN WALLED CYST
FILLED WITH STRAW COLOURED WATERY
FLUID
 EXTERNAL SURFACE IS
SEMITRANSLUCENT, SMOOTH
 IT MAY BE LESS THAN 1 CM TO AS MUCH
AS 30 CM IN DIAMETER
MICROSCOPIC EXAMINATION
 IT IS LINED BY PROPERLY ORIENTED LOW
COLUMNAR EPITHELIUM WHICH IS
CILIATED AND RESEMBLES TUBULE
EPITHELIUM

 MICROSCOPIC PAPILLAE MAY BE FOUND


MUCINOUS CYSTADENOMA
 MUCINOUS CYSTADENOMA ALSO ARISES
FROM SURFACE EPITHELIUM OF OVARY
BUT ARE LESS COMMON THAN SEROUS
CYSTADENOMA
 THEY OCCUR PRINCIPALLY IN MID ADULT
LIFE & ARE RARE BEFORE PUBERTY &
AFTER MENOPAUSE
 BILATERAL INVOLVEMENT IS RARE &
OCCURS IN 5% CASES
GROSS
 THEY ARE LARGER THAN SEROUS
TUMOURS
 THEY ARE TYPICALLY MULTILOCULAR
 THIN WALLED CYST WITH SMOOTH
EXTERNAL SURFACE CONTAINING
STICKY, VISCID, GELATINOUS FLUID RICH
IN GLYCOPROTEIN
 LOCULI VARY IN SIZE & OFTEN TUMOUR
MAY BE COMPOSED OF ONE MAJOR
CAVITY WITH MANY DAUGHTER CYST
MICROSCOPIC EXAMINATION
 IT IS CHARACTERISED BY LINING OF NON
CILIATED, TALL, COLUMNAR EPITHELIUM
CELLS WITH BASAL NUCLEI & APICAL
MUCINOUS VACUOLES SIMILAR TO
BENIGN CERVICAL & INTESTINAL
EPITHELIUM
 THERE IS VERY LITTLE TENDENCY TO
PAPILLARY PROLIFERATION OF THE
EPITHELIUM
GESTATIONAL AND PLACENTAL DISORDERS

 Diseases of pregnancy and pathologic conditions


of the placenta are important causes of
intrauterine or perinatal death, congenital
malformations, intrauterine growth retardation,
maternal death, and a great deal of morbidity for
both mother and child.
 The placenta is composed of chorionic villi that
sprout from the chorion to provide a large contact
area between the fetal and maternal circulations.
HYDATIFORM MOLE
 It is characterised histologically by cystic
swelling of chorionic villi
 Accompanied by variable trophoblastic
proliferation
 In the past, most patients presented with 4-5
months of pregnancy with vaginal bleeding
 Nowadays, they are diagnosed earlier due to
regular ultrasound
 H. mole may be invasive & non invasive
 Two types of non invasive moles-
 1.Complete/ classic mole
 2.Partial mole
CLINICAL FEATURES.

 Most women with partial and early complete moles


present with spontaneous pregnancy loss or undergo
curettage because of abnormalities in ultrasound
showing diffuse villous enlargement.
 In complete moles quantitative analysis of human
chorionic gonadotropin (HCG) shows levels of hormone
greatly exceeding those produced during a normal
pregnancy of similar gestational age.
 The vast majority of moles are removed by thorough
curettage.
COMPLETE MOLE
 IN THIS, ALL OR MOST OF THE VILLI ARE
EDEMATOUS & THERE IS
CIRCUMFERENTIAL PROLIFERATION

 THE CYTOLOGICAL STUDY SHOWS


DIPLOID PATTERN (44XX) IN 90% CASES
PARTIAL MOLE
 IN THIS, SOME VILLI SHOW EDEMATOUS
CHANGES WHILE OTHER ARE NORMAL

 TROPHOBLASTIC PROLIFERATION IS
FOCAL

 THE KARYOTYPE IS MOSTLY TRIPLOID


GROSS
 UTERINE CAVITY IS FILLED WITH
DELICATE FRIABLE MASSES OF THIN
WALLED TRANSLUCENT CYSTIC GRAPE
LIKE STRUCTURES

 FOETAL PARTS ARE SEEN IN PARTIAL


MOLE NOT IN COMPLETE MOLE
MICROSCOPIC EXAMINATION
 IN PARTIAL MOLE, VILLOUS EDEMA INVOLVES
PORTION OF VILLI
 THE TROPHOBLASTIC PROLIFERATION IS FOCAL
 IN COMPLETE MOLE, HYDROPIC CHANGES
INVOLVE MOST OF THE VILLI & THERE IS
ABSENCE OF VASCULATURE IN THESE VILLI
 THE CIRCUMFERENTIAL PROLIFERATION OF
TROPHOBLASTIC CELLS PRODUCES SHEETS &
MASSES OF CELLS
 IN COMPLETE MOLE, BOTH
SYNCYTIOTROPHOBLAST &
CYTOTROPHOBLASTS ARE
PROLIFERATING WHEREAS IN PARTIAL
MOLE, SYNCYTIOTROPHOBLASTS ARE
PROLIFERATING

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