Weaver Joshua, Bergfeld Wilma F
Department of Anatomic Pathology, The Cleveland Clinic, Cleveland, OH 44195, USA.
Arch Pathol Lab Med. 2009 Sep;133(9):1490-4. doi: 10.5858/133.9.1490.
Grover disease, also known as transient acantholytic dermatosis, is a papulovesicular rash of the upper trunk, generally among older white males; it is usually pruritic but temporary. Grover disease is characterized by 4 different acantholytic histologic patterns, and it has been associated with numerous disorders, including hematologic malignancies. Follow-up and treatment are often difficult to evaluate secondary to the spontaneous remittance and occasional fluctuant course of the disease. Our objective will be to discuss the diagnostic considerations of Grover disease and focus on the postulated pathogenesis, including concurrent disorders and the role of the pathologist in examining skin biopsies of this nonhereditary vesicobullous disorder. Although recognized as a common condition, Grover disease's pathogenesis still remains unknown. Because Grover disease has been associated frequently with other dermatologic and nondermatologic skin conditions, inspection for other pathologic processes within the skin biopsy is essential to rule out other concomitant disorders, including hematopoietic malignancies.
格罗弗病,也称为暂时性棘层松解性皮肤病,是一种发生在上胸部的丘疹水疱性皮疹,多见于老年白人男性;通常伴有瘙痒,但为暂时性。格罗弗病具有4种不同的棘层松解组织学模式,并且与多种疾病相关,包括血液系统恶性肿瘤。由于该病有自发缓解和偶尔波动的病程,随访和治疗往往难以评估。我们的目的是讨论格罗弗病的诊断要点,并重点关注其假定的发病机制,包括并发疾病以及病理学家在检查这种非遗传性水疱大疱性疾病的皮肤活检中的作用。尽管格罗弗病被认为是一种常见疾病,但其发病机制仍然不明。由于格罗弗病经常与其他皮肤病和非皮肤病相关,因此在皮肤活检中检查其他病理过程对于排除其他并发疾病(包括造血系统恶性肿瘤)至关重要。