Eccrine Spiradenoma (ES) is an exceedingly rare sweat-gland tumor, it usually presents as a solitary lesion and painful nodule. ES is a kind of neoplasm with distinct histological characteristics and nonspecific clini...Eccrine Spiradenoma (ES) is an exceedingly rare sweat-gland tumor, it usually presents as a solitary lesion and painful nodule. ES is a kind of neoplasm with distinct histological characteristics and nonspecific clinical manifestations. Most ES cases have a benign course;however, malignant transformation would occur after a long period of latency. The diagnosis mostly depends on the clinic symptom, histological features and immunohistochemistry. Here, we report a case of ES and literature review. The aim of this study is to understand clinic and histological features for ES.展开更多
Giant Vascular Eccrine Spiradenoma (GVES) is a rare variant of Eccrine Spiradenoma (ES), a tumor that develops from the sweat gland. It differs from Eccrine Spiradenoma in its larger size and vascularity as well as pr...Giant Vascular Eccrine Spiradenoma (GVES) is a rare variant of Eccrine Spiradenoma (ES), a tumor that develops from the sweat gland. It differs from Eccrine Spiradenoma in its larger size and vascularity as well as propensity for bleeding and ulceration, which may cause a clinical misdiagnosis of vascular lesion or malignant tumor. All previously reported cases in English literature have been in older adults and the elderly, age range being from 49 to 84 years. Here a rare case of GVES in a young male presenting as a cutaneous chest wall lesion with bleeding, which was initially diagnosed as a vascular lesion clinically as well as on histopathology is reported.展开更多
IntroductionEccrine spiradenoma (ES) is an uncommon adnexal tumor that is thought to originate from eccrine sweat glands.ES usually manifests as a blue-violet or florid solitary painful nodule with pain on palpation.E...IntroductionEccrine spiradenoma (ES) is an uncommon adnexal tumor that is thought to originate from eccrine sweat glands.ES usually manifests as a blue-violet or florid solitary painful nodule with pain on palpation.ES may affect any part of the body,but mostly affects the extremities without age and sex predilection.Multiple ES lesions are rarely documented.The typical pathological features,namely,small cells with hyperchromatic nuclei and large cells with dark nuclei,help with diagnosis and differentiation of ES from other painful skin tumors.Malignant transformation is rarely reported.Surgical excision is the most recommended treatment and provides a good prognosis.Here we report a rare multiple ES case with zosteriform presentation,and the patient had nothing crucial were out of normal limits including dermatological examination and routine investigations.展开更多
文摘Eccrine Spiradenoma (ES) is an exceedingly rare sweat-gland tumor, it usually presents as a solitary lesion and painful nodule. ES is a kind of neoplasm with distinct histological characteristics and nonspecific clinical manifestations. Most ES cases have a benign course;however, malignant transformation would occur after a long period of latency. The diagnosis mostly depends on the clinic symptom, histological features and immunohistochemistry. Here, we report a case of ES and literature review. The aim of this study is to understand clinic and histological features for ES.
文摘Giant Vascular Eccrine Spiradenoma (GVES) is a rare variant of Eccrine Spiradenoma (ES), a tumor that develops from the sweat gland. It differs from Eccrine Spiradenoma in its larger size and vascularity as well as propensity for bleeding and ulceration, which may cause a clinical misdiagnosis of vascular lesion or malignant tumor. All previously reported cases in English literature have been in older adults and the elderly, age range being from 49 to 84 years. Here a rare case of GVES in a young male presenting as a cutaneous chest wall lesion with bleeding, which was initially diagnosed as a vascular lesion clinically as well as on histopathology is reported.
文摘IntroductionEccrine spiradenoma (ES) is an uncommon adnexal tumor that is thought to originate from eccrine sweat glands.ES usually manifests as a blue-violet or florid solitary painful nodule with pain on palpation.ES may affect any part of the body,but mostly affects the extremities without age and sex predilection.Multiple ES lesions are rarely documented.The typical pathological features,namely,small cells with hyperchromatic nuclei and large cells with dark nuclei,help with diagnosis and differentiation of ES from other painful skin tumors.Malignant transformation is rarely reported.Surgical excision is the most recommended treatment and provides a good prognosis.Here we report a rare multiple ES case with zosteriform presentation,and the patient had nothing crucial were out of normal limits including dermatological examination and routine investigations.
