Malignant pilomatricoma is a cutaneous condition characterized by a locally aggressive tumor composed of hair-matrix cells.[2]: 671 [3]
Signs and symptoms
Malignant pilomatricoma usually manifests as a single firm, painless, movable, asymptomatic dermal or subcutaneous lump. It has been shown that the underlying skin can become ulcerated and exhibit severe discoloration; the latter is thought to be one of the few significant indicators of cancer.[4] The head, neck, and back are frequent locations of occurrence. Their sizes range from 1 to 10 cm.[5]
Diagnosis
Grossly, removed tumors frequently have a grayish appearance, are cystoid, encapsulated, and have viscous fluids.[6][7] Histologically, there is an abrupt shift to eosinophilic ghost or shadow cells (anucleate matrical corneocytes), which are characterized by a prominent proliferation of basaloid cells with ample transparent cytoplasm.[8] Seldom do basaloid cells palisade or contain melanin; instead, they aggregate into nests, bands, and amorphous sheets.[7][9] There are calcification and ulceration scattered across the cell types.[10][11] The basaloid cells' nuclei exhibit pleomorphism, frequent aberrant mitoses, and a high apoptotic index.[6][8][12] The diagnosis is strongly supported by ulceration and infiltration into adnexal structures; some reports even establish a correlation between these findings and the degree of malignancy.[13] Usually, a lymphohistiocytic infiltration and dense desmoplastic stroma are found next to the tumor capsule.[7][8]
Treatment
Malignant pilomatricoma is a low grade malignant tumor that is locally aggressive. Therefore, sufficient surgical clearance is necessary to stop localized recurrence.[14]
Outlook
The initial treatment strategy and the diagnosis of the suspicious lesion are the primary factors influencing the overall outcome in malignant pilomatricoma. Lesions that were treated with simple excision resurfaced locally in 50–83 percent of instances, but lesions that were broadly excised returned in 18–23 percent of patients. In 10 to 16 percent of patients, there were metastases, which usually damaged pulmonary or lymphatic organs. Seven to nine percent of patients reported a death related to malignant pilomatricoma, either directly or indirectly.[4]
Epidemiology
As of 2022 about 130 cases have been reported in English literature.[15]
^ abcHardisson, David; Linares, M. Dolores; Cuevas-Santos, Jesús; Contreras, Félix (2001). "Pilomatrix Carcinoma: A Clinicopathologic Study of Six Cases and Review of the Literature". The American Journal of Dermatopathology. 23 (5). Ovid Technologies (Wolters Kluwer Health): 394–401. doi:10.1097/00000372-200110000-00002. ISSN0193-1091. PMID11801770. S2CID20213287.
^ abcHerrmann, Jennifer L.; Allan, Adam; Trapp, Kara M.; Morgan, Michael B. (2014). "Pilomatrix carcinoma: 13 new cases and review of the literature with emphasis on predictors of metastasis". Journal of the American Academy of Dermatology. 71 (1). Elsevier BV: 38–43.e2. doi:10.1016/j.jaad.2014.02.042. ISSN0190-9622. PMID24739254.
^Otero, Mario N.; Trujillo, Carolina P.; Parra-Medina, Rafael; Morales, Samuel D. (2017). "Metastatic Malignant Pilomatrixoma in an 8-Year-Old Girl Misdiagnosed as a Recurrent Pilomatrixoma". The American Journal of Dermatopathology. 39 (3). Ovid Technologies (Wolters Kluwer Health): e41–e43. doi:10.1097/dad.0000000000000736. ISSN0193-1091. PMID27673386. S2CID31624894.
^Melancon, Jeffrey M.; Tom, Wynnis L.; Lee, Robert A.; Jackson, Michelle; Brian Jiang, Shang I. (2011). "Management of Pilomatrix Carcinoma: A Case Report of Successful Treatment with Mohs Micrographic Surgery and Review of the Literature". Dermatologic Surgery. 37 (12). Ovid Technologies (Wolters Kluwer Health): 1798–1805. doi:10.1111/j.1524-4725.2011.02170.x. ISSN1076-0512. PMID22093235. S2CID34659885.
^Lazar, Alexander J. F.; Calonje, Eduardo; Grayson, Wayne; Dei Tos, Angelo P.; Mihm, Martin C.; Redston, Mark; McKee, Phillip H. (2004-12-15). "Pilomatrix carcinomas contain mutations in CTNNB1, the gene encoding β-catenin". Journal of Cutaneous Pathology. 32 (2). Wiley: 148–157. doi:10.1111/j.0303-6987.2005.00267.x. ISSN0303-6987. PMID15606674. S2CID84712278.
^Cornejo, Kristine M.; Deng, April (2013). "Pilomatrix Carcinoma". The American Journal of Dermatopathology. 35 (3). Ovid Technologies (Wolters Kluwer Health): 389–394. doi:10.1097/dad.0b013e318274b7da. ISSN0193-1091. PMID23221469.
^Karaaslan, Onder; Can, Murat Melih; Silistreli, Ayse Ozlem Karatas; Bedir, Yagmur Kaan; Caliskan, Gorkem (2012). "Malignant Pilomatrixoma Arising on the Previously Irradiated Face: Case Report and Literature Review". Journal of Cutaneous Medicine and Surgery. 16 (5). SAGE Publications: 341–343. doi:10.1177/120347541201600511. ISSN1203-4754. PMID22971309. S2CID39266289.
NISHIOKA, Megumi; TANEMURA, Atsushi; YAMANAKA, Takashi; TANI, Mamori; MIURA, Hiroyuki; ASAKURA, Makiko; TAMAI, Nobuyuki; KATAYAMA, Ichiro (2010-07-22). "Pilomatrix carcinoma arising from pilomatricoma after 10-year senescent period: Immunohistochemical analysis". The Journal of Dermatology. 37 (8). Wiley: 735–739. doi:10.1111/j.1346-8138.2010.00887.x. ISSN0385-2407. PMID20649718. S2CID12113484.
Aherne, NJ; Fitzpatrick, DA; Gibbons, D; Collins, CD; Armstrong, JG (2009). "Recurrent malignant pilomatrixoma invading the cranial cavity: Improved local control with adjuvant radiation". Journal of Medical Imaging and Radiation Oncology. 53 (1). Wiley: 139–141. doi:10.1111/j.1754-9485.2009.02049.x. ISSN1754-9477. PMID19453540. S2CID26386969.