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Dec 2020 DOI 10.14302/issn.2474-7785.jarh-20-3628
Syiao Wei NgCorresponding author
Hospital Sultanah Aminah, Jalan Persiaran Abu Bakar Sultan, 80100 Johor Bahru, Johor, Malaysia
Multiple primary malignancies especially in the head and neck region is no longer a rare occurrence and the prevalence is increasing. They were described as synchronous when the malignancies present within 6 months of another or metachronous tumors if the subsequent malignancy presents 6 months late…
Feb 2018 DOI 10.14302/issn.2639-1716.jn-18-1965
Jamie T. CaraccioloCorresponding author
Lipomatous tumors are among the most common primary musculoskeletal neoplasms affecting both pediatric and adult patient populations. Patient age, tumor location, and imaging features all contribute to the differential diagnosis of musculoskeletal tumors. Tumors identified outside of common patient…
Dec 2017 DOI 10.14302/issn.2576-6694.jbbs-17-1869
Rita de Cassia StoccoCorresponding author
Introduction Bovine papillomavirus (BPV) is the etiological agent of bovine papillomatosis, infectious and neoplastic disease, characterized by the presence of multiple papillomas that can regress spontaneously or to persist and progress to malignancies when in association with environmental cofacto…
Aug 2017 DOI 10.14302/issn.2470-5020.jnrt-17-1530
Robert SusloCorresponding author
It is crucial for the society, the government and the medical community to retrieve the full and reliable statistical information on malignant brain neoplasms (C71-C71.9 ICD-10) to adjust the medical financing, staff and equipment properly. In order to retrieve information useful for public health p…
Jun 2017 DOI 10.14302/issn.2470-5020.jnrt-17-1529
Jaroslaw DrobnikCorresponding author
Epidemiological data concerning malignant neoplasms of meninges and central nervous system parts other than brain in Poland are reported to many medical databases run by various institutions and are incongruent with each other which makes their practical interpretation highly difficult. Data on regi…
Jun 2015 DOI 10.14302/issn.2576-182X.jbsc-14-576
Tejpal GuptaCorresponding author
Multi-modality therapy has led to significant improvement in outcomes for childhood medulloblastoma; however, long-term survivors have become more susceptible to late effects of therapy including induction of second malignant neoplasms and even remain at an increased risk of late relapses including…
Mar 2022 DOI 10.14302/issn.2641-5518.jcci-22-4097
Julian Iñaki L. GarciaCorresponding author
Malignant melanoma the most common malignancies associated with GI involvement. They usually manifest clinically at an advanced stage of neoplasm. Surgery is also recommended for palliative treatment of GIT metastases. A case of a 67-year-old male diagnosed with malignant melanoma for 7 months had b…
May 2021 DOI 10.14302/issn.2689-5773.jcdp-21-3799
Anubha BajajCorresponding author
Preface Frequently, benign bone tumours are an incidental discovery wherein clinical symptoms are contingent to tumour location and magnitude and manifest as localized pain, swelling, skeletal deformities or pathologic fracture. Radiographic imaging is a cogent methodology of discerning the neoplasm…
Jan 2021 DOI 10.14302/issn.2689-5773.jcdp-20-3648
Anubha BajajCorresponding author
Angiomatoid fibrous histiocytoma (AFH) is an exceptional, soft tissue neoplasm of indeterminate lineage and intermediate malignancy associated with minimal localized tumour reoccurrence and infrequent distant metastasis. Preliminarily contemplated to be a variant or derivative of malignant fibrous…
Nov 2020 DOI 10.14302/issn.2689-5773.jcdp-20-3577
Anubha BajajCorresponding author
Low grade fibromyxoid sarcoma (LGFMS) is an exceptional, low grade, soft tissue sarcoma with indolent biological behaviour, extensive preclinical stage, enhanced localized tumour reoccurrence and delayed, distant metastasis. As the deceptively benign neoplasm was initially scripted by Evans in 1987…
Sep 2020 DOI 10.14302/issn.2689-5773.jcdp-20-3512
Anubha BajajCorresponding author
Parachordoma is an extremely exceptional, peripherally situated soft tissue neoplasm arising at non axial locations. Also designated as soft tissue “myoepithelioma” or “mixed tumour”, the tumefaction histologically simulates a chordoma of axial skeleton and was referred to as “central chordoma” emer…
Sep 2020 DOI 10.14302/issn.2689-5773.jcdp-20-3506
Anubha BajajCorresponding author
Preface Fibromatosis colli is an exceptional, benign neoplasm of infancy constituted by spindle-shaped cells of sternocleidomastoid muscle. Fibromatosis colli emerges within specific sites such as distal or inferior segment of sternocleidomastoid muscle and is accompanied by diffuse enlargement of t…
Sep 2020 DOI 10.14302/issn.2372-6601.jhor-20-3552
Xin QingCorresponding author
Plasma cell neoplasms of the thyroid gland are uncommon. They may occur either as a primary extraosseous (extramedullary) plasmacytoma or as secondary involvement by multiple myeloma (MM). Here, we report the case of a 62-year-old female, presenting with goiter and Hashimoto’s thyroiditis, in whom t…
Sep 2020 DOI 10.14302/issn.2471-2175.jdrt-20-3511
Anubha BajajCorresponding author
Intravascular papillary endothelial hyperplasia is an exceptional, benign, inflammatory, vascular neoplasm delineating papillary configuration engendered from reactive proliferation of damaged endothelial cells, while being confined to a thrombus. Initially scripted by Pierre Mason in 1923, the tume…
Apr 2020 DOI 10.14302/issn.2689-5773.jcdp-20-3292
Anubha BajajCorresponding author
Perineurioma is an exceptional, benign neoplasm entirely composed of neoplastic perineurial cells and arises from the peripheral nerve. Pertaining to location, the neoplasm predominantly demonstrates configurations such as intra-neural or extra-neural, confined to the soft tissue. Perineurioma was i…
Apr 2020 DOI 10.14302/issn.2372-6601.jhor-20-3293
Selcuk DemiralCorresponding author
Objective Meningiomas are most common intracranial benign tumors comprising around one third of all intracranial neoplasms, and typically have benign and indolent nature with slow-growing behaviour. Benign meningiomas are slow growing tumors typically following an indolent disease course. Neverthele…
Feb 2020 DOI 10.14302/issn.2689-5773.jcdp-20-3218
Anubha BajajCorresponding author
Trichoepithelioma is a benign, cutaneous neoplasm originating from the hair follicle and is categorized into singular trichoepithelioma, multiple trichoepithelioma and desmoplastic trichoepithelioma wherein desmoplastic trichoepithelioma is cogitated as an exceptional, cutaneous adnexal tumour. Des…
Feb 2020 DOI 10.14302/issn.2690-4837.ijip-20-3176
Anubha BajajCorresponding author
Multiple endocrine neoplasia type 1 (MEN1) is a syndrome emerging from characteristic mutations of MEN1 gene with concurrently enunciated multiple endocrine and tumours and associated non-endocrine neoplasm. Previously designated as Werner’s syndrome, MEN1 syndrome denominates genomic mutation wit…
Dec 2019 DOI 10.14302/issn.2575-1212.jvhc-19-3101
Pamela Rodrigues Reina MoreiraCorresponding author
Papillary carcinoma is a mammary neoplasia of women and female dogs characterized by papillary fibrovascular projections lined by epithelial cells. Evaluation on the biology of these tumors can be done by immunohistochemistry through detection of alpha-smooth muscle actin protein in the papillary my…
Jul 2019 DOI 10.14302/issn.2689-5773.jcdp-19-2890
Anubha BajajCorresponding author
Initially described by Pinkus and Mehregan in 1963 as an epidermotropic eccrine carcinoma, eccrine porocarcinoma cogitates an exceptional sweat gland malignancy. Eccrine porocarcinoma was adapted as a nomenclature by Mishisma and Morikoin in 1969. The neoplasm is a malignant analogue of eccrine por…