Ovarian fibrothecoma with minor sex cord elements: a case report

Ovarian fibroma is the most common sex cord stromal tumour of ovary accounting to 1-5% of all ovarian tumours. Minor sex cord elements in ovarian fibroma are a rare entity occupying less than 10% of tumour area. To the best of our knowledge only 20 cases has been reported till date. This case is presented because of its rarity. Authors reported a case of fibrothecoma with minor sex cord elements in a 70yr old postmenopausal women who presented with postmenopausal bleeding with abdominal mass.

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Anorectal Gastrointestinal Stromal Tumour: A Case Treated with Radical Surgery

Journal of Nepal Health Research Council ◽

10.3126/jnhrc.v16i1.19376 ◽

2018 ◽

Vol 16 (1) ◽

pp. 99-101

Author(s):

Arbin Joshi

Keyword(s):

Case Report ◽

Radical Surgery ◽

Anal Verge ◽

Gastrointestinal Stromal Tumour ◽

Stromal Tumour ◽

Rare Entity ◽

Good Recovery ◽

Rectal Pain ◽

Close Proximity ◽

Firm Mass

Gastrointestinal Stromal Tumour involving rectum and anal canal is an extremely rare entity. This is a case report of a 47 years lady presented with fresh rectal bleed associated with rectal pain and foul smelling rectal mucus discharge. On rectal examination, she had a firm mass palpable about 1.5 cm from anal verge. Considering the size of the tumour and its close proximity with cervix and involvement of levator muscles, extralevator abdominal perineal excision of rectum was undertaken with good recovery after surgery. It was followed by imatinib therapy.

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Dysgermgerminoma in a 14 year old girl: a case report

International Journal of Reproduction Contraception Obstetrics and Gynecology ◽

10.18203/2320-1770.ijrcog20170605 ◽

2017 ◽

Vol 6 (3) ◽

pp. 1149

Author(s):

V. N. Kurude ◽

Sukanya Thorat

Keyword(s):

Case Report ◽

Abdominal Mass ◽

Cell Tumor ◽

Accurate Diagnosis ◽

Abdominal Distention ◽

Ovarian Mass ◽

Lower Abdomen ◽

Loss Of Weight ◽

Ovarian Tumours ◽

Ovarian Dysgerminoma

An accurate diagnosis of ovarian dysgerminoma is crucial as, as its management differs from other ovarian tumours. We report a case of ovarian dyegerminoma in a 14 year old girl who presented with abdominal distention. Examination revealed a huge intra-abdominal mass causing displacement of bowel loops laterally. On ultrasound, a solid heterogeneously hyperechoic lesion of size 18 x 9.4 cm with few cystic and necrotic areas within most likely, left adnexa reaching upto the umbilicus and shows vascularity within both ovaries not seen separately from the lesion. On CT (A+P), a heterogenous hypodense polycystic mass of size 8.5x1.4x16.7 with multiple irregular hypodensities seen in the lower abdomen and pelvis. The mass was removed after laparotomy under general anaesthesia. Finally, the diagnosis of ovarian germ cell tumor (Dysgerminoma was made. Present case presented with marked abdominal distention, without any loss of weight, appetite or any menstrual problem. Such a presentation may be unusual for such a large malignant ovarian mass.

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Gastrointestinal stromal tumour presenting as palpable abdominal mass: A rare entity

World Journal of Gastrointestinal Surgery ◽

10.4240/wjgs.v7.i6.98 ◽

2015 ◽

Vol 7 (6) ◽

pp. 98

Author(s):

Manoj R Bhambare

Keyword(s):

Abdominal Mass ◽

Gastrointestinal Stromal Tumour ◽

Stromal Tumour ◽

Rare Entity ◽

Palpable Abdominal Mass

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A rare case of uterine leiomyosarcoma: A case report

Indian Journal of Obstetrics and Gynecology Research ◽

10.18231/j.ijogr.2021.082 ◽

2021 ◽

Vol 8 (3) ◽

pp. 404-407

Author(s):

Bhuvana Preethi ◽

Usha Rajesh ◽

Mala Vijayakrishnan

Keyword(s):

Smooth Muscle ◽

Case Report ◽

Smooth Muscle Cells ◽

Postmenopausal Women ◽

Malignant Tumor ◽

Rare Case ◽

Muscle Cells ◽

Uterine Leiomyosarcoma ◽

Postmenopausal Bleeding

Uterine leiomyosarcoma is a rare malignant tumor that arises from smooth muscle cells. It comprises of 1% of all uterine malignancy. We report a case of 54 year old Postmenopausal women with 2 episodes of postmenopausal bleeding and was diagnosed with Leiomyosarcoma of uterus.

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A Rare Entity of Gastrointestinal Stromal Tumour Arising from a Meckel’s Diverticulum: a Case Report

Journal of Gastrointestinal Cancer ◽

10.1007/s12029-017-9920-2 ◽

2017 ◽

Vol 49 (3) ◽

pp. 351-354

Author(s):

Kshitij Manerikar ◽

Iqbal Ali ◽

Chandradip Patil ◽

Mirat Dholakia ◽

Pratham Mody

Keyword(s):

Case Report ◽

Meckel’S Diverticulum ◽

Gastrointestinal Stromal Tumour ◽

Meckel's Diverticulum ◽

Stromal Tumour ◽

Rare Entity

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RARE PRESENTATION OF HUGE CERVICAL FIBROID –CASE REPORT

10.36106/2000579 ◽

2021 ◽

pp. 16-17

Author(s):

Rujuta fuke ◽

Monika singh

Keyword(s):

Ovarian Cancer ◽

Coming Out ◽

Abdominal Mass ◽

The Body ◽

Surgical Removal ◽

Rare Entity ◽

Postmenopausal Bleeding ◽

Provisional Diagnosis ◽

Rare Presentation ◽

Rare Tumours

Most of the leiomyomas are situated in the body of uterus. Fibroids arising from cervix are rare tumours accounting for 2% of all broids. Cervical leiomyomata are mostly single and are subserous or interstitial in origin. Generally these tumors present with retention of urine, constipation, sensation of something coming out of vagina and rarely at times present with abdominal mass which may mimic ovarian cancer. We report a case of 55 yr. married patient with complaints of something coming out of vagina and postmenopausal bleeding of short duration. Provisional diagnosis was a huge cervical broid protruding through the introitus on examination. Vaginal hysterectomy was done for patient along with removal of cervical broid which was conrmed on histopathology as leiomyoma. Conclusion: Huge cervical broids are rare entity and treatment is surgical removal.

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