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Glomus tumor is a rare benign neoplasm, accounting for less than 2% of all the soft tissue tumors. Although they can develop in any part of the body, they commonly do so in upper extremities, most commonly in fingers. Here, we report two cases of glomus tumor at rare locations, in order to...
Memoirs in scientific journals, by mandate or custom, are less personal and largely factual. This recollection of Dr D D Patel’s life could provide glimpses of the person behind the personality.
Perivascular epithelioid cell tumor (PEComa) is a tumor of mesenchymal origin, with features of perivascular epithelioid cells. The primary sites of PEComa reported are the uterus, vulva, rectum, heart, breast, urinary bladder, abdominal wall, pancreas, retroperitoneum, liver, and uterus. But...
Postmastectomy seroma formation is a common and notorious problem that every treating surgeon frequently faces in the management of patients with breast cancer. Several technical modifications and innovations have been proposed to either overcome or reduce its occurrence. One such method tested...
This study was conducted among patients with adrenocortical carcinoma (ACC) to analyze their clinico-pathological profile, management outcomes, and risk factors for local recurrence, systemic metastasis, and survival. The data of patients with ACC who were managed at a single institution between...
Peutz-Jeghers syndrome (PJS) is an autosomal dominant familial hamartomatous polyposis syndrome characterized by multiple gastrointestinal hamartomatous polyps and mucocutaneous melanin pigmentation. We report two cases, with no family history, presenting as emergency, one with perforation...
Squamous cell carcinoma constitutes around 95% of malignancies in the oral cavity. The 5-year overall survival has not substantially improved for oral cancers over the last few decades, despite several advances in diagnosis, imaging, and treatment modalities. With progressive improvement in...
A Correction to this paper has been published: https://doi.org/10.1007/s13193-021-01470-x
Clear cell chondrosarcoma is a rare subtype of chondrosarcoma, included in the category of low-grade (grade 1) sarcomas of the bone. We evaluated the results of treatment of these rare tumours at our institute and documented their outcomes in a hitherto unreported ethnic (Asian) cohort. Of the...
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