Biography
Abhimanyu Grover is a Resident of Patiala, Punjab, India. He has graduated from Government Medical College and Hospital, Amritsar. After completion of Internship, he was commissioned as a Medical Officer in the Indian Air Force at the rank of Flight Lieutenant in December 2009. He has served in the Indian Armed Forces for a period of eight years and four months and completed his tenure as a Short Service Commissioned Officer, in April 2018. Currently, he is pursuing his Post-graduation in Pathology, at Kalinga Institute of Medical Sciences and PBMH, Bhubaneswar, Odisha, India.
Abstract
Background: Bullous systemic lupus erythematosus (BSLE) is a rare autoimmune disease characterized by generalized bullous eruption. It is a unique bullous disease phenotype characterized by with distinctive clinical features of tense bullae involving the sun-exposed areas and confirmed on histologically by subepidermal bullae with predominantly polymorphic infiltrate. Immunopathological features reveal immunoglobulin and complement deposition at dermoepidermal junction. Case report: Twenty seven (27) -year- old female presented with fever, myalgia, arthralgia, fatigue, vesiculobullous skin eruptions, oral ulcers since two months. The vesiculobullous lesions were primarily localized at the forehead, lower part of face and front of neck. Laboratory investigations revealed a positive ANA, raised anti-dsDNA titre, low serum C3 and C4 levels with anemia (Hb 6.1 g/dl). On histological examination subepidermal bullae with neutrophilic infiltration and karyorrhectic debris in the epidermal layers were seen. Direct IF revealed dermoepidermal deposition of IgG and C3. The patient was diagnosed as Bullous systemic lupus erythematosus (BSLE). She was treated with dapsone and was cured completely. Conclusion: BSLE is an uncommon condition. It requires good clinical acumen to differentiate it from similar conditions and prompt investigations for quick diagnosis as it responds very well to treatment.
Biography
Vigyan Mishra is currently pursuing his Post-graduate, MD Pathology at Kalinga Institute of Medical Science, KIIT University, Bhubaneswar, Odisha, India. After completing his MBBS from RD Gardi Medical College, Ujjain, Madhya Pradesh, India, and he served in under National Rural Health Mission at Anuppur district, Madhya Pradesh, India and developed interest in Pathology. Currently, he is working on his first scientific initiation and a two years prospective study on “Expression of Cyclin D1 and p53 in Oral Squamous Cell Carcinomaâ€.
Abstract
Endometrial stromal sarcoma (ESS) is a rare neoplasm comprising 0.2% of all uterine malignancies. Though synchronous ESS and bilateral ovarian endometrioid adenocarcinoma is documented but to the best of our knowledge this is the first case of synchronous ESS and bilateral serous adenocarcinoma of ovary. A 48-year-old female presented with pain in lower abdomen and irregular bleeding per vaginum. Sonography revealed bulky uterus. Hysterectomy with bilateral salpingectomy was done. Gross: Large polypoid mass within endometrial cavity. Microscopy: Nests and islands of uniform, bland looking tumor cells permeating into the myometrium. Foci of adenomyos are also seen. Tumor cells were CD10 positive. A diagnosis of low grade ESS was made. Subsequent CT scan was unremarkable. Bilateral oophorectomy was done. Grossly both the ovaries appear normal. Microscopy: Small foci of tumor present beneath the surface of each ovary. Tumor cells were arranged in papillary, glandular and cribriform pattern with high grade nuclear morphology and good number of mitosis. Cells were CK7, CA125 and WT1 positive. Diagnosis: Low grade endometrial stromal sarcoma with synchronous bilateral serous adenocarcinoma of ovary. Endometriosis is a known risk factor for neoplasm. Possible association between these entities may be due to malignant transformation of adenomyosis and endometriosis.