Icthyosis Uteri with in Situ Carcinoma

Report of 2 Cases

Authors

  • Almas Iqbal Pathan Byramjee Jeejeebhoy Government Medical College and Sassoon General Hospitals, Pune India
  • Jyoti Kiran Kudrimoti Byramjee Jeejeebhoy Government Medical College and Sassoon General Hospitals, Pune India
  • Shaila Chandrakant Puranik Byramjee Jeejeebhoy Government Medical College and Sassoon General Hospitals, Pune India

DOI:

https://doi.org/10.21276/apalm.2166

Keywords:

Dysplasia, CIN, pyometra, Hysterectomy

Abstract

Icthyosis uteri is a rare condition in which entire surface of the endometrium is replaced by stratified squamous epithelium. Two cases of Icthyosis uteri are reported for their rarity. The first case was of a 70 year old female with a history of lower abdominal pain and white PV (per vaginal) discharge since 3 months. The second case was of a 70 year old female with history of PV (per vaginal) spotting and breathlessness since 1 year. Gross examination of uterine cavity showed rough and irregular endometrial surface in the first case while in second case endometrium was atrophic. Microscopy of endometrium in both cases revealed total replacement of endometrial glands by stratified squamous epithelium with changes of in situ carcinoma or severe dysplasia. Cervix also showed severe dysplasia or CIN (cervical intra epithelial neoplasia) III in both the cases.

Author Biographies

Almas Iqbal Pathan, Byramjee Jeejeebhoy Government Medical College and Sassoon General Hospitals, Pune India

Department of  Pathology

Jyoti Kiran Kudrimoti, Byramjee Jeejeebhoy Government Medical College and Sassoon General Hospitals, Pune India

Department of Pathology

Shaila Chandrakant Puranik, Byramjee Jeejeebhoy Government Medical College and Sassoon General Hospitals, Pune India

Department of Pathology

References

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Published

29-11-2018

How to Cite

1.
Pathan AI, Kudrimoti JK, Puranik SC. Icthyosis Uteri with in Situ Carcinoma: Report of 2 Cases. Ann of Pathol and Lab Med [Internet]. 2018 Nov. 29 [cited 2024 Nov. 23];5(11):C172-174. Available from: https://pacificejournals.com/journal/index.php/apalm/article/view/2166

Issue

Section

Case Report