Parra Izquierdo Viviana, Frias-Ordoñez Juan, Romero-Sanchez Consuelo, Alvarado Julio, Florez Cristian
Hospital Internacional de Colombia, BUCARAMANGA, Colombia.
Clínica de Marly, Bogota, Colombia.
Am J Gastroenterol. 2021 Dec 1;116(Suppl 1):S12. doi: 10.14309/01.ajg.0000798792.71403.36.
Background: Metastatic Crohn's disease (MCD) is an unusual cutaneous manifestation in Crohn's disease (CD), and concomitant oral and vulvar involvement is even more unusual. It can debut with cavity lesions oral such as canker sores, ulcers, lip edema, granulomatosis, dry mouth, abscesses in the salivary ducts, erythema, gingivitis, glossitis, among others, however, simultaneous compromise with several oral lesions and so severe with loss of multiple pieces dental is very rare.
Patient in the fourth decade of life with a family history of autoimmunity who debuts with severe oral manifestations with a requirement for extraction of 14 teeth, severe gingivitis, smooth tongue and glossitis, aphthous stomatitis, ulcers, lip edema and angular cheilitis, without clear cause, and in management by the oral pathology group. Associated with this, there was vulvo-perineal compromise with ulcerated, inflammatory, erythematous and infiltrated lesions. It was initially suspected of Behçet's disease, HLA B51 was performed, it was negative, also, negative pathergy test, and no other suggestive systemic findings. A vulvar biopsy was performed with marked edema of the dermis, dilated lymphatics with perivascular and interstitial lymphoplasmacytic infiltrate and noncaseating granulomas, negative for microorganisms. At this level, it was compatible with MCD, without presence of gastrointestinal symptoms and calprotectin levels in stool in normal range. High and low endoscopic studies and capsule endoscopy were performed in small intestine, without alterations, it was managed by dermatology with topical steroids and by dentistry with dental implants. It was considered patient with inflammatory bowel disease (IBD) type CD with severe extraintestinal manifestations (EIM), although it did not present compromise intestinal treatment, it was decided to start treatment with anti-TNF initially with adalimumab developing paradoxical psoriasis, later treatment with infliximab, again with presentation of severe paradoxical psoriasis, for which it was suspended. Cyclosporine was also used as an immunomodulator, presenting intolerable tachycardia. 18 months after these symptoms, she presented episcleritis of the left eye and begins with colicky abdominal pain and average diarrheal stools 5-a-day, it was performed high and low endoscopic studies without alterations and new capsule endoscopic of small intestine documenting Crohn's enteritis involving the duodenum, jejunum and ileum, considering a patient with IBD type CD, with EIM with vulvo-perineal compromise, severe oral involvement and episcleritis. Currently is under management with azathioprine and Ustekinumab, with clinical improvement significant.
MCD represents a diagnostic challenge, it can debut without gastrointestinal involvement, and its clinical and histopathological findings simulate other entities. A timely diagnosis is required to seek early benefit in the patient.
背景:转移性克罗恩病(MCD)是克罗恩病(CD)一种不常见的皮肤表现,同时累及口腔和外阴则更为罕见。它可能以口腔病变首发,如口腔溃疡、溃疡、唇部水肿、肉芽肿病、口干、唾液腺脓肿、红斑、牙龈炎、舌炎等,然而,同时出现多种口腔病变且严重到导致多颗牙齿脱落的情况非常罕见。
患者为中年,有自身免疫性疾病家族史,首发严重口腔表现,需要拔除14颗牙齿,伴有严重牙龈炎、光滑舌和舌炎、复发性阿弗他口炎、溃疡、唇部水肿和口角炎,无明确病因,由口腔病理组负责诊治。与此相关的是,外阴 - 会阴出现溃疡、炎症、红斑和浸润性病变。最初怀疑为白塞病,进行了HLA B51检测,结果为阴性,同时,针刺反应试验也为阴性,且无其他提示性的全身表现。进行了外阴活检,显示真皮明显水肿,淋巴管扩张,血管周围和间质有淋巴细胞和浆细胞浸润,无干酪样肉芽肿,微生物检测为阴性。在这一阶段,诊断符合MCD,无胃肠道症状,粪便钙卫蛋白水平在正常范围内。对小肠进行了上下消化道内镜检查和胶囊内镜检查,未发现异常,由皮肤科用局部类固醇治疗,牙科用牙种植体治疗。该患者被认为是患有严重肠外表现(EIM)的CD型炎症性肠病(IBD),尽管未出现肠道受累情况,但决定最初使用抗TNF药物阿达木单抗治疗,结果出现了矛盾性银屑病,后来改用英夫利昔单抗治疗,再次出现严重的矛盾性银屑病,因此停药。还使用了环孢素作为免疫调节剂,但出现了无法耐受的心动过速。这些症状出现18个月后,她出现了左眼巩膜炎,并开始出现绞痛性腹痛和每天平均5次的腹泻性大便,再次进行上下消化道内镜检查未发现异常,新的小肠胶囊内镜检查记录了克罗恩肠炎累及十二指肠、空肠和回肠,考虑该患者为患有EIM、外阴 - 会阴受累、严重口腔受累和巩膜炎的CD型IBD。目前正在使用硫唑嘌呤和优特克单抗进行治疗,临床症状有显著改善。
MCD是一个诊断难题,它可以在无胃肠道受累的情况下首发,其临床和组织病理学表现可模拟其他疾病。需要及时诊断以便为患者争取早期治疗效果。