|| Print ISSN: 2589-7837 || Online ISSN: 2581-3935 || International Journal of Medical Science and Diagnosis Research (IJMSDR) Available Online at www.ijmsdr.com NLM (National Library of Medicine ID: 101738824) Original Research Article Volume 5, Issue 11; November:2021; Page No. 17-20 17 | Page Eccrine Angiomatous Hamartoma: A Rare Presentation in Late Adulthood Zeany Cheran Momin 1 , Veena Gupta 2 , Gauri Munjal 3 , Rahul Jakhar 4 , Chandershekhar Yadav 5 , Sunita Singh 6 1 Resident, Pt. B. D. Sharma PGIMS, Rohtak 2 Professor, Pt. B. D. Sharma PGIMS, Rohtak 3 Senior Resident, Pt. B. D. Sharma PGIMS, Rohtak 4 Resident, Pt. B. D. Sharma PGIMS, Rohtak 5 Resident, Pt. B. D. Sharma PGIMS, Rohtak 6 Sr. Professor and Head, Pt. B. D. Sharma PGIMS, Rohtak Conflicts of Interest: Nil Corresponding author: Zeany Cheran Momin DOI: https://doi.org/10.32553/ijmsdr.v5i11.870 Abstract: Eccrine angiomatous hamartoma is a tumor characterized by benign malformation of eccrine and vascular elements, occurring generally at birth or during early infancy and childhood. The rarity with which it is encountered in adults and the elderly makes it a diagnostic challenge in such age brackets. We report an interesting case of eccrine angiomatous hamartoma presenting in late adulthood confirmed by histopathology. Keywords: Cisplatin, concurrent chemotherapy, daily, weekly, three weekly, carcinoma cervix Introduction: Eccrine angiomatous hamartoma (EAH) is a rare, benign lesion histologically characterized by hyperplastic eccrine and vascular structures which may also be associated with proliferation of other dermal elements like hair follicles and adipose tissues. EAH was first described by Lotzbeck in 1859 and the term was coined by Hyman et al in 1968 [1,2] . It arises at birth or appears in early childhood, with only a handful of reports of adult onset lesions documented in literature. Case Report: A 57-year-old male patient presented with complaints of swelling on the second toe of right foot for duration of one year. It was gradually progressive in size. There was no history of local trauma, hypertrichosis, hyperhidrosis, any systemic illnesses or similar swelling in any other part of the body. Patient denied history of similar lesions in his family. Local examination showed an ill-defined swelling measuring approximately 4cm x 2.5cm which was soft and non-tender. The overlying skin was normal. His routine blood parameters were within normal limits. An ultrasonogram of the swelling revealed a cystic lesion with few internal septations showing no significant flow on color doppler. CEMR right foot revealed a lobulated cystic lesion on superior aspect of second digit (also extending along medial margin) overlying proximal and middle phalanges, being hypointense on T1W and hyperintense on T2W images with slight peripheral enhancement on CEMR and rim hypointense on T2W images which was thin and regular. A clinical and