Related ArticlesFocal Mass-Forming Autoimmune Pancreatitis Mimicking Pancreatic Cancer: Which strategy? Tunis Med. 2019 May;97(5):731-735 Authors: Hedfi M, Charfi M, Nejib FZ, Benlahouel S, Debaibi M, Ben Azzouz S, Bouhawala MH, Chouchene A Abstract Autoimmune pancreatitis (AIP) is a rare form of chronic pancreatitis that predominantly affects men in their fifth and sixth decades and often presents with obstructive jaundice and pancreatic enlargement....
Fri May 01, 2020 13:19
Related ArticlesUnilateral MALT conjunctival lymphoma: a case report. Tunis Med. 2019 May;97(5):726-730 Authors: Elleuch IE, Sayadi S, Daldoul A, Kharat M, Zbiba W Abstract INTRODUCTION: The conjunctival localization of MALT-type lymphoma is rare although it is the most common tumor of the ocular adnexa. OBSERVATION: We report a case of a 57 years old female patient who presented with a unilateral primitive MALT lymphoma, confined to the conjunctiva,...
Fri May 01, 2020 13:19
Related ArticlesGiant Desmoid-Type Fibromatosis of the Neck: A Very Rare Infiltrating Tumor. Ear Nose Throat J. 2019 Oct-Nov;98(9):549-550 Authors: Lechien JR, Briganti G, Aubain NS, Dequanter D, Rodriguez A PMID: 31722569 [PubMed - indexed for MEDLINE]
Fri May 01, 2020 13:19
Related ArticlesSeborrheic Keratosis in the Auricle: A Rare Tumor. Ear Nose Throat J. 2019 Oct-Nov;98(9):560-561 Authors: Hong CE, Kim Y, Choi HS, Jeong J Abstract Seborrheic keratosis (SK) is a common, benign, cutaneous skin tumor of the elderly patients. It is commonly observed in the head, neck, trunk, and extremities except the palms and soles. Its occurrence in the auricle has been reported even more rarely than in external auditory canal. We experienced...
Fri May 01, 2020 13:19
Related ArticlesA Dual-Targeting Functionalized Graphene Film for Rapid and Highly Sensitive Fluorescence Imaging Detection of Hepatocellular Carcinoma Circulating Tumor Cells. ACS Appl Mater Interfaces. 2019 Dec 04;11(48):44999-45006 Authors: Wu C, Li P, Fan N, Han J, Zhang W, Zhang W, Tang B Abstract High recurrence and metastasis rates are the major causes of the high mortality of hepatocellular carcinoma (HCC). Circulating tumor cells (CTCs) disseminating...
Fri May 01, 2020 13:19
Related Articles[Pancreatoblastoma in a pediatric patient: a case report]. Rev Gastroenterol Peru. 2019 Jul-Sep;39(3):302-306 Authors: Verastegui S R, Gonzales DP, Compén Chang PDR, De la Cruz L, Alarcón O A Abstract Pancreoblastoma is a very rare tumor that originates from the exocrine epithelial cells of the pancreas. However, it is the most frequent pancreatic tumor in children. It usually appears in the first decade of life with an average of 5 years...
Fri May 01, 2020 13:19
Related Articles[Duodenal type folicular lymphoma: case report and literature review]. Rev Gastroenterol Peru. 2019 Jul-Sep;39(3):276-279 Authors: Castro D, Beltrán B, Quiñones MDP, Palomino E, Cotrina E, Alva E, Bryan Medina J, Yábar A Abstract Duodenal type follicular lymphoma is a rare malignancy accounting for less than 4% of primary non-Hodgkin lymphomas of the gastrointestinal tract and it is a new entity that was recently described in the new...
Fri May 01, 2020 13:19
Related ArticlesGiant perianal condyloma acuminatum in an infant without sexual abuse. Arch Pediatr. 2019 Nov;26(8):473-474 Authors: Elfatoiki FZ, Hali F, Baghad B, Marnissi F, Chiheb S Abstract Giant condyloma acuminatum is rare in infants. We report a case of giant perianal condyloma in a 10-month-old infant without sexual abuse. The patient was treated by surgical excision associated with electrocoagulation with no recurrence after 2 years. While...
Fri May 01, 2020 13:19
Related ArticlesClinical and radiological characteristics of patients with retroperitoneal infantile hemangiomas. Pediatr Dermatol. 2019 Nov;36(6):823-829 Authors: Peterman CM, Gibson RS, Lillis AP, Fishman SJ, Liang MG Abstract BACKGROUND: Infantile hemangiomas (IHs) are the most common tumors of infancy. The objective was to identify clinical and radiological patterns in patients with retroperitoneal IHs. METHODS: We reviewed patients from...
Fri May 01, 2020 13:19
Related ArticlesShould we biopsy melanonychia striata in Asian children? A retrospective observational study. Pediatr Dermatol. 2019 Nov;36(6):864-868 Authors: Colin Tan W, Wang DY, Seghers AC, Koh MJA, Nicholas Goh SG, Joyce Lee SS Abstract BACKGROUND AND OBJECTIVES: Melanonychia striata is common in children of darker-skinned Asian races, while subungual melanoma is extremely rare and it is difficult to make a diagnosis clinically. However, performing...
Fri May 01, 2020 13:19
Related ArticlesA giant superinfected uterine angioleiomyoma with distant septic metastases: an extremely rare presentation of a benign process and a systematic review of the literature. Arch Gynecol Obstet. 2019 10;300(4):841-847 Authors: Sánchez-Iglesias JL, Capote S, Cubo-Abert M, Carbonell-Socias M, Cabrera S, Illán-Hernández L, Pérez-Benavente MA, Monreal-Clua S, Gil-Moreno A Abstract PURPOSE: Uterine angioleiomyoma is a rare type of leiomyoma...
Fri May 01, 2020 13:19
Related ArticlesCongenital eccrine angiomatous hamartoma: Expanding the morphologic presentation and a review of the literature. Pediatr Dermatol. 2019 Nov;36(6):909-912 Authors: Smith SD, DiCaudo DJ, Price HN, Andrews ID Abstract Eccrine angiomatous hamartoma (EAH) is a rare benign vascular hamartoma characterized histologically by an increased size and number of mature eccrine glands associated with multiple foci of dilated capillaries in the dermis...
Fri May 01, 2020 13:19
Related ArticlesPigmented Villonodular Synovitis Presenting as Unilateral Hearing Loss: Review of the Literature and Case Report. ORL J Otorhinolaryngol Relat Spec. 2019;81(2-3):171-182 Authors: Brant JA, Kaufman AC, Luu N, Grady SM, O Apos Malley BW, Ruckenstein MJ Abstract BACKGROUND/AIMS: To review the existing literature on pigmented villonodular synovitis (PVNS) of the temporomandibular joint (TMJ) and report a rare case of PVNS of the TMJ presenting...
Fri May 01, 2020 13:19
Related ArticlesTenosynovial giant cell tumor of the cervical spine: a case report. Spinal Cord Ser Cases. 2019;5:23 Authors: Furuhata R, Iwanami A, Tsuji O, Nagoshi N, Suzuki S, Okada E, Fujita N, Yagi M, Matsumoto M, Nakamura M, Watanabe K Abstract Introduction: Tenosynovial giant cell tumors (TSGCTs) generally occur in the limb joints, and only rarely in the spine. This case report describes a patient with TSGCT of the spine at C1-C2, which was treated...
Fri May 01, 2020 13:19
Related ArticlesTumor-proximal liquid biopsy to improve diagnostic and prognostic performances of circulating tumor cells. Mol Oncol. 2019 09;13(9):1811-1826 Authors: Buscail E, Chiche L, Laurent C, Vendrely V, Denost Q, Denis J, Thumerel M, Lacorte JM, Bedel A, Moreau-Gaudry F, Dabernat S, Alix-Panabières C Abstract Circulating tumor cell (CTC) detection and numeration are becoming part of the common clinical practice, especially for breast, colon,...
Fri May 01, 2020 13:19
Related ArticlesDiabetes-mediated promotion of colon mucosa carcinogenesis is associated with mitochondrial dysfunction. Mol Oncol. 2019 09;13(9):1887-1897 Authors: Del Puerto-Nevado L, Santiago-Hernandez A, Solanes-Casado S, Gonzalez N, Ricote M, Corton M, Prieto I, Mas S, Sanz AB, Aguilera O, Gomez-Guerrero C, Ayuso C, Ortiz A, Rojo F, Egido J, Garcia-Foncillas J, Minguez P, Alvarez-Llamas G, DiabetesCancerConnect Consortium Abstract Type 2 diabetes...
Fri May 01, 2020 13:19
Related ArticlesSeizures in patients with a phaeochromocytoma/paraganglioma (PPGL): A review of clinical cases and postulated pathological mechanisms. Rev Neurol (Paris). 2019 Oct;175(9):495-505 Authors: Li Y, Zhang B Abstract The purpose of this work was to expound on the postulated pathological mechanisms through which pheochromocytoma/paraganglioma (PPGL) can cause seizures by conducting a comprehensive review of ten cases and several pathogenic...
Fri May 01, 2020 13:19
Related ArticlesPlasmacytoid Myoepithelioma of Palate Heading Toward Malignancy: A Rare Case With Immunohistochemical Analysis. Ear Nose Throat J. 2019 Oct-Nov;98(9):551-553 Authors: Devi A, Kamboj M, Narwal A, Bhagol A PMID: 30909738 [PubMed - indexed for MEDLINE]
Fri May 01, 2020 13:19
Related ArticlesLinitis plastica of the colon due to metastases of invasive lobular breast carcinoma. Rev Esp Enferm Dig. 2019 Apr;111(4):326-328 Authors: Viso Vidal D, Villanueva Pavón R, Jorquera Plaza F Abstract Colon metastases from breast carcinoma are relatively rare and the invasive lobular subtype tends to metastasize more frequently due to its peritoneal dissemination. A 67-year-old female with a lobular subtype breast neoplasm was treated...
Fri May 01, 2020 13:19
Related ArticlesClinicopathological Features of ALK Expression in 9889 Cases of Non-small-Cell Lung Cancer and Genomic Rearrangements Identified by Capture-Based Next-Generation Sequencing: A Chinese Retrospective Analysis. Mol Diagn Ther. 2019 06;23(3):395-405 Authors: Zhao R, Zhang J, Han Y, Shao J, Zhu L, Xiang C, Zhang Q, Teng H, Qin G, Zhao L, Ye M, Zhao J, Ding W Abstract BACKGROUND: The clinicopathological features and genomic rearrangements...
Fri May 01, 2020 13:19
Related ArticlesSolitary bone plasmacytoma compression injury disguised as back pain: a case report. Spinal Cord Ser Cases. 2019;5:16 Authors: Jackson SD, Wiering BA, Herrmann AA, Hinz MA, Hanson LR Abstract Introduction: Low back pain is a leading disability worldwide; however, it is not often the result of a serious underlying condition such as a tumor. As a result, diagnosis of a serious underlying cause of low back pain may be delayed, such as in...
Fri May 01, 2020 13:19
Related ArticlesCharacteristics of mismatch repair deficiency in sarcomas. Mod Pathol. 2019 07;32(7):977-987 Authors: Doyle LA, Nowak JA, Nathenson MJ, Thornton K, Wagner AJ, Johnson JM, Albrayak A, George S, Sholl LM Abstract Due to the efficacy of immune checkpoint inhibitor therapy in tumors with deficient mismatch repair, there has been a surge in demand for mismatch repair deficiency testing in various tumor types. Mismatch repair deficiency is...
Fri May 01, 2020 13:19
Related ArticlesPrimary malignant melanoma of esophagus: clinicopathologic characterization of 20 cases including molecular genetic profiling of 15 tumors. Mod Pathol. 2019 07;32(7):957-966 Authors: Lasota J, Kowalik A, Felisiak-Golabek A, Zięba S, Waloszczyk P, Masiuk M, Wejman J, Szumilo J, Miettinen M Abstract Primary malignant melanoma of esophagus is very rare, and its clinicopathologic and genetic features have not been extensively investigated....
Fri May 01, 2020 13:19
Related ArticlesPrevalence of recurrent oncogenic fusion in mismatch repair-deficient colorectal carcinoma with hypermethylated MLH1 and wild-type BRAF and KRAS. Mod Pathol. 2019 07;32(7):1053-1064 Authors: Wang J, Yi Y, Xiao Y, Dong L, Liang L, Teng L, Ying JM, Lu T, Liu Y, Guan Y, Pang J, Zhou L, Lu J, Zhang Z, Liu X, Liang X, Zeng X, Yi X, Zhou W, Xia X, Yang L, Zhang J, Kopetz S, Futreal PA, Wu H, Liang Z Abstract Oncogenic fusions are rare in colorectal...
Fri May 01, 2020 13:19
Diagnosis and rehabilitation of a pregnant woman with spinal cord disorder due to spinal cord tumor.
Related ArticlesDiagnosis and rehabilitation of a pregnant woman with spinal cord disorder due to spinal cord tumor. Spinal Cord Ser Cases. 2019;5:8 Authors: Bitterman J, Donovan J, Lam M Abstract Introduction: Spinal cord tumors are a rare cause of spinal cord disorder (SCD). Early diagnosis can be challenging, especially in patient populations with other potential etiologies for back pain, such as pregnant women. Case presentation: A 28-year-old...
Fri May 01, 2020 13:19
Related Articles[Secondary pseudopriapism after lymphatic invasion in a patient with adenocarcinoma of the rete testis]. Rev Int Androl. 2019 Jan - Mar;17(1):37-40 Authors: Scott Pabon G, Fiter Gómez L, Manzano Peña MT Abstract We present a case, the first ever published to our knowledge, of penile metastasis from rete testis adenocarcinoma. 62 years old male, who underwent orchiectomy for left testicular mass. Pathology results reveal rete testis adenocarcinoma....
Fri May 01, 2020 13:19
Related ArticlesA rare MYC/BCL3 double-translocation and protein-expression in a diffuse large B-cell lymphoma. Leuk Lymphoma. 2019 03;60(3):825-828 Authors: Ohno H, Nakagawa M, Kishimori C, Fukutsuka K, Hayashida M, Izumi K, Akasaka T, Honjo G, Haga H PMID: 30187810 [PubMed - indexed for MEDLINE]
Fri May 01, 2020 13:19
Related ArticlesA Rare Pediatric Case of Posttraumatic Pseudoaneurysm: Case Report and Literature Review. Pediatr Emerg Care. 2019 Dec;35(12):e226-e228 Authors: Gu A, Kam AJ Abstract Posttraumatic pseudoaneurysms are extremely rare in pediatric populations. In many cases, pseudoaneurysms may be confused with abscesses, epidermoid cysts, arteriovenous fistula, foreign objects, and ganglion cysts, as well as tumors. They are associated with distinguishing...
Fri May 01, 2020 13:19
Related ArticlesEnrichment of Kinase Fusions in ESR1 Wild Type, Metastatic Breast Cancer Revealed by a Systematic Analysis of 4,854 Patients. Ann Oncol. 2020 Apr 26;: Authors: Ross DS, Liu B, Schram AM, Razavi P, Lagana SM, Zhang Y, Scaltriti M, Bromberg JF, Ladanyi M, Hyman DM, Drilon A, Zehir A, Benayed R, Chandarlapaty S, Hechtman JF Abstract BACKGROUND: Kinase fusions are rare and poorly characterized in breast cancer. We aimed to characterize kinase...
Thu Apr 30, 2020 14:12
Related ArticlesNovel Diagnostic Methods and Posttreatment Clinical Phenotypes Among Intracranial Germ Cell Tumors. Neurosurgery. 2020 Apr 29;: Authors: Takami H, Perry A, Graffeo CS, Giannini C, Daniels DJ Abstract BACKGROUND: Central nervous system (CNS) germ cell tumors (GCT) are rare and complex pediatric neoplasms, the optimal management of which remains an area of active investigation. OBJECTIVE: To present an updated cohort study, with...
Thu Apr 30, 2020 14:12
Related ArticlesAssociation of Rare Pathogenic DNA Variants for Familial Hypercholesterolemia, Hereditary Breast and Ovarian Cancer Syndrome, and Lynch Syndrome With Disease Risk in Adults According to Family History. JAMA Netw Open. 2020 Apr 01;3(4):e203959 Authors: Patel AP, Wang M, Fahed AC, Mason-Suares H, Brockman D, Pelletier R, Amr S, Machini K, Hawley M, Witkowski L, Koch C, Philippakis A, Cassa CA, Ellinor PT, Kathiresan S, Ng K, Lebo M, Khera AV Abstract...
Thu Apr 30, 2020 14:12
Related ArticlesPost-traumatic Sacral Epidermoid Cyst Masquerading as Chordoma on Imaging: A Case Report. JNMA J Nepal Med Assoc. 2020 Mar;58(223):192-194 Authors: Phuyal S, Prabhakar A, Balasundaram P, Gaikwad P Abstract Intradural spinal epidermoid cysts are rare, benign lesions either acquired from trauma, surgery, lumbar puncture or arise as congenital lesions, particularly associated with spinal dysraphism. Epidermoid cyst arising from the spine...
Thu Apr 30, 2020 14:12
Related ArticlesRare case of venous tumour thrombus from acinic cell carcinoma of the parotid gland. Ann R Coll Surg Engl. 2020 Apr 29;:e1-e6 Authors: Yap D, Dragan A, Weller A, Tatla T Abstract Head and neck tumour thrombus is a rare pathology and at present there are no reported cases of tumour thrombus secondary to acinic cell carcinoma of the parotid gland. We report a case of an 81-year-old man with an acinic cell carcinoma of the left parotid and...
Thu Apr 30, 2020 14:12
Related ArticlesRectal leiomyoma robotic enucleation - A video vignette. Colorectal Dis. 2020 Apr 29;: Authors: Paolini C, Checcacci P, Tribuzi A, Menegatti B, Annecchiarico M, Moraldi L, Coratti A Abstract Leiomyomas are by definition benign tumours of smooth muscle and are usually found in the uterus. Less frequently they are located along the digestive tract. Rectal leiomyoma is a rare entity, comprising about 0.03 to 0.05% of all rectal tumours....
Thu Apr 30, 2020 14:12
Related ArticlesPaediatric acute lymphoblastic leukaemia and caesarean section: A report from the United Kingdom Childhood Cancer Study (UKCCS). Paediatr Perinat Epidemiol. 2020 May;34(3):344-349 Authors: Bonaventure A, Simpson J, Ansell P, Roman E Abstract BACKGROUND: Reports have suggested that children born by caesarean initiated before labour onset may be at increased risk of developing acute lymphoblastic leukaemia (ALL). However, with most data...
Thu Apr 30, 2020 14:12
Related ArticlesIntraosseous Schwannoma: Case Report and Review of the Literature. Rev Bras Ortop (Sao Paulo). 2020 Apr;55(2):258-262 Authors: Drumond GC, Nakagawa SA, Costa FD, de Souza MYT, Comunello J, Chung WT Abstract Schwannoma is a benign neural sheath tumor of the soft tissue, and its intraosseous presentation is very rare. It is estimated that intraosseous schwannomas represent 0.2% of all bone tumors. The tumor may affect any site of the skeleton,...
Thu Apr 30, 2020 13:10
Related ArticlesMixed neuroendocrine-non-neuroendocrine neoplasms (MiNEN) of pancreas: a rare entity-worth to note. BMJ Case Rep. 2020 Apr 27;13(4): Authors: Varshney B, Bharti JN, Varshney VK, Yadav T Abstract Mixed adenocarcinoma with neuroendocrine tumour of pancreas has been reported infrequently and consists of both epithelial and neuroendocrine component. We encountered an 81-year-old male patient who presented with clinical features of painful...
Thu Apr 30, 2020 13:10
Related ArticlesCentromeric cohesion failure invokes a conserved choreography of chromosomal mis-segregations in pancreatic neuroendocrine tumor. Genome Med. 2020 Apr 28;12(1):38 Authors: Quevedo R, Spreafico A, Bruce J, Danesh A, El Ghamrasni S, Giesler A, Hanna Y, Have C, Li T, Yang SYC, Zhang T, Asa SL, Haibe-Kains B, Krzyzanowska M, Smith AC, Singh S, Siu LL, Pugh TJ Abstract BACKGROUND: Pancreatic neuroendocrine tumors (PANETs) are rare, slow growing...
Thu Apr 30, 2020 13:10
Related ArticlesA scoping review and proposed workflow for multi-omic rare disease research. Orphanet J Rare Dis. 2020 Apr 28;15(1):107 Authors: Kerr K, McAneney H, Smyth LJ, Bailie C, McKee S, McKnight AJ Abstract BACKGROUND: Patients with rare diseases face unique challenges in obtaining a diagnosis, appropriate medical care and access to support services. Whole genome and exome sequencing have increased identification of causal variants compared to...
Thu Apr 30, 2020 13:10
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