Browsing by Author "Shashikant Patne"

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18F-fluorodeoxyglucose positron emission tomography/computed tomography findings of osteoblastoma of rib-A rare benign tumor with unusual site and uncommon age
(Wolters Kluwer Medknow Publications, 2021) Shantanu Pande; Venkata Mohan Gollamudi; Shashikant Patne; Mukta Ramadwar; Nilendu Purandare
Osteoblastoma accounts for approximately 1% of all primary bone tumors. We report F18-fluorodeoxyglucose positron emission tomography/computed tomography (F18-FDG PET/CT) findings of an osteoblastoma in the rib of a 20-month-old girl child, who had fever with pain in the right shoulder for 4 months. This lesion was initially judged as a malignant bone tumor but a biopsy revealed it to be an osteoblastoma. The age of patient and predominant site of disease involvement contributes to uniqueness of our case. In our case, F18-FDG PET/CT has facilitated biopsy planning and ruled out other sites of disease involvement. © 2021 Wolters Kluwer Medknow Publications. All rights reserved.
Chondroid lipoma in a child
(2008) Shashikant Patne; N. Aryya; A. Gangopadhyay
Chondroid lipoma (CL), a rare lipoma variant, has not been described well for patients younger than 14 years of age. We herein report an extremely unusual instance of CL in a 7-year-old child. The cut surface of the tumor showed peculiar tan-brown and yellow-white areas. Histopathological sections showed the presence of eosinophilic variably vacuolated round- to oval-spindle cells in a myxo-hyaline background. The findings were consistent with CL. The case is reported because of its extreme rarity.
Co-existence of Diffuse Serous Cystadenoma and Pancreatic Neuroendocrine Tumor
(Springer India, 2017) Mallika Tewari; Shashikant Patne; Richa Katiyar; Dipanjan Biswas; Hs Shukla
Diffuse serous cystic neoplasm (SCN) associated with pancreatic neuroendocrine tumor (PNET) is a rare finding reported previously in only three patients to the best of our knowledge. We herein present one such interesting report of a diffuse serous cystic adenoma (SCA) and co-existent PNET in a 25-year old lady who presented with abdominal pain for past 6 months. A triple-phase pancreatic protocol computed tomography (CT) scan revealed multiple cysts involving the entire pancreas. The cysts were thin walled, ranging from 2 to 8 cm in width, with no calcification or central scar that was confirmed at laparotomy. A frozen section revealed a neuroendocrine tumor and she underwent total pancreatectomy. Diffuse SCA with co-existent PNET infiltrating nerve bundles of the pancreatic parenchyma was made upon histopathology further verified by chromogranin-A immunostaining. The patient is insulin dependent and doing well at 2 years of follow-up. The origin of endocrine tumors from multipotent ductular stem cells has been suggested. © 2017, Association of Surgeons of India.
Epithelioid leiomyoma of vagina
(2010) Mohan Kumar; Lubna Sadaf; Shivanjali Raghuvanshi; Shashikant Patne
Leiomyoma is the most common benign mesenchymal tumor of the vagina. However, leiomyoma with epithelioid features are very uncommon in the vagina. We report a rare case of epithelioid variant of leiomyoma in a 40-year old woman who presented with a painless vaginal mass. Immunohistochemistry against smooth muscle actin was done for confirmation. © Internet Scientific Publications, LLC., 1996 to 2010.
Hemoglobin E disorders in Eastern Uttar Pradesh
(2009) Shashikant Patne; Jyoti Shukla
The distribution of hemoglobin E (α2β 226Glu→Lys) is mostly restricted to Northeastern India. While evaluating the patients of jaundice, we came across two cases of hemoglobin E (Hb E) disorders. The first case is in a 22-year-old Bengali male and the second case of Hb E/βthalassemia in a 5-year-old Hindu boy. The family study revealed Hb E trait in both the parents of Case 1, whereas in Case 2, the father was found to have Hb E trait and the mother had β-thalassemia minor, thus confirming the diagnosis. Herein, we present the laboratory diagnosis and comparative data of the spectrum of Hb E disorders (i.e., heterozygous Hb E trait, homozygous Hb E disease and compound heterozygous Hb E/β-thalassemia) that was found in our index cases and their parents.
Orofacial granulomatosis affecting lip and gingiva in a 15-year-old patient: A rare case report
(Wolters Kluwer Medknow Publications, 2015) Monika Bansal; Nootan Singh; Shashikant Patne; Satyendra Kumar Singh
Orofacial granulomatosis (OFG) is a rare disorder affecting the orofacial region, and clinically characterized by diffuse, nontender, soft to firm, painless swelling restricted to one or both lips and intraoral sites such as tongue, gingiva and buccal mucosa. Histologically, OFG is characterized by noncaseating granulomatous inflammation. The early diagnosis of OFG is essential for the better prognosis of the lesion. Delay in diagnosis of OFG results into formation of indurated and permanent swelling of the lip that not only compromises esthetic appearance but also causes impairment in function such as speaking and eating. Early diagnosis of OFG is challenging to the health care professionals due to clinical and histological resemblance to other chronic granulomatous disorders. Thus, dentists may act as a first person to diagnose the lesion and play an important role in the multidisciplinary treatment of granulomatous disorders. Here, we present a case of OFG affecting lips and gingiva in a 15-year-old patient without any identifiable systemic or local causes.
Primary high-grade testicular leiomyosarcoma
(2009) Mohan Kumar; Shashikant Patne; Sandip Kumar; V. Shukla
We herein present an extremely rare occurrence of primary intratesticular leiomyosarcoma. A 65-year-old patient presented with painless enlargement of the right testis. A high inguinal orchiectomy was done. Histopathological examination of the excised mass was consistent with high-grade leiomyosarcoma. Pertinent literature is reviewed and the importance of excluding the germ cell tumor and the paratesticular neoplasm is emphasized.
Simultaneous appearance of dual malignancies of hematopoietic system-multiple myeloma and acute myeloid leukemia
(2008) Jyoti Shukla; Shashikant Patne; N. Singh; Usha
We herein report a case of denovo and simultaneous appearance of multiple myeloma and acute myeloid leukemia in a 58-year-old female patient, without prior exposure to chemotherapy or radiotherapy. This case is reported because of its extreme rarity.