Pock Lumír, Stuchlík David, Hercogová Jana
Dermatopathological Laboratory, Department of Dermatology, District Hospital Pardubice, Prague, Czech Republic.
Int J Dermatol. 2006 Dec;45(12):1408-11. doi: 10.1111/j.1365-4632.2006.02919.x.
Crystal storing histiocytosis (CSH) imitating rhabdomyoma is a very rare disease entity involving different tissues. The skin is involved in extremely rare cases.
To describe the clinical and histopathological characteristics in a patient with unusually extensive skin involvement.
A 62-year-old woman presented with a large red infiltrated verrucosus lesion on the anterior aspect of the chest and on the neck. The skin biopsy revealed histiocytes throughout the whole dermis containing thin crystalloid structures in the cytoplasm. Upon histopathological examination, crystal-storing histiocytosis was diagnosed and consequently a hematological examination revealed multiple myeloma IgG Kappa. Skin involvement by CSH proceeded the diagnosis of multiple myeloma by 4 years.
Phagocytosis of crystals of immunoglobulins by histiocytes (crystals storing histiocytosis) is a rare symptom associated most often with lymphoproliferative disease. The clinical picture is not characteristic, in the histopathologic picture it is striking similarity to rhabdomyoma. The skin involvement by crystal storing histiocytosis can be the first symptom of malignant lymphoma that can proceed the hematological malignancy by years.
模仿横纹肌瘤的晶体贮积性组织细胞增多症(CSH)是一种涉及不同组织的非常罕见的疾病实体。皮肤受累极为罕见。
描述一名皮肤受累异常广泛的患者的临床和组织病理学特征。
一名62岁女性,胸部前方和颈部出现一个巨大的红色浸润性疣状病变。皮肤活检显示整个真皮层有组织细胞,其细胞质中含有细小的晶体结构。经组织病理学检查,诊断为晶体贮积性组织细胞增多症,随后血液学检查显示多发性骨髓瘤IgG κ型。CSH皮肤受累比多发性骨髓瘤诊断早4年。
组织细胞吞噬免疫球蛋白晶体(晶体贮积性组织细胞增多症)是一种罕见症状,最常与淋巴增殖性疾病相关。临床表现不具有特征性,在组织病理学表现上与横纹肌瘤有惊人的相似性。晶体贮积性组织细胞增多症的皮肤受累可能是恶性淋巴瘤的首发症状,可在血液系统恶性肿瘤出现前数年出现。