Extramedullary plasmocytoma associated with a massive deposit of amyloid in the duodenum.

We report a rare case of extramedullary plasmocytoma associated with a massive deposit of amyloid in the duodenum. A 72-year-old Japanese man was admitted to our hospital presenting with a 3-mo history of epigastric pain, vomiting and weight loss. On computed tomography (CT) a wall thickening of the fourth part of the duodenum was observed. Multiple biopsies obtained from the lesion showed infiltration of plasma cells and lymphocytes, but they were not conclusive. The patient underwent resection of the lesion and, on histopathological examination, the lesion consisted of a dense and diffuse infiltrate of plasma cells and a few admixed lymphocytes with reactive follicles extending to the muscular propria. An extensive deposition of amyloid was also observed. Immunohistochemical stains revealed that a few plasmacytoid cells showed lambda light chain staining, though most were kappa light chain positive. These cells also were positive for CD138 and CD56 but negative for CD20 and CD79. The findings were consistent with extramedullary plasmocytoma associated with a massive deposit of amyloid in duodenum. A subsequent workup for multiple myeloma was completely negative. The patient showed no signs of local recurrence or dissemination of the disease after 12 mo follow-up. Because of the association of plasmocytoma and amyloidosis, the patient must be followed up because of the possible systemic involvement of the neoplasm and amyloidosis in future.

[Vitiligoid hypopigmented macules and tumor of the follicular infundibulum]. / Máculas hipopigmentadas vitiligóides e tumor do infundíbulo folicular.

Tumor of the follicular infundibulum is an uncommon cutaneous lesion with different forms of clinical presentation, namely solitary and multiple/eruptive variants. The former shows predilection for head and neck and presents as a papulonodular scaly tumor. The latter is less frequent and occurs on facial, neck and upper chest areas as brown, reddish or more commonly hypopigmented macules leading to the differential diagnosis with vitiligo. The different clinical forms share the same histopathologic aspect. The present report describes a case of the multiple variant of tumor of the follicular infundibulum disclosing facial vitiligoid macules in a 35-year-old male patient.

Máculas hipopigmentadas vitiligóides e tumor do infundíbulo folicular / Vitiligoid hypopigmented macules and tumor of the follicular infundibulum

Tumor do infundíbulo folicular é lesão cutânea incomum, com várias formas de apresentação clínica. Destacam-se as formas solitária e eruptiva/múltipla. A primeira apresenta-se como lesão papulonodular descamativa em região de cabeça e pescoço. A segunda, alvo deste relato, é mais rara, ocorrendo em face, pescoço e porção superior do tronco como lesões maculares pardas, avermelhadas ou, mais frequentemente, hipopigmentadas, podendo levar ao diagnóstico diferencial com lesões vitiligóides. A apresentação microscópica das diferentes formas clínicas é similar. Neste artigo, relatamos um caso de tumor do infundíbulo folicular múltiplo/eruptivo apresentando-se como máculas vitiligóides faciais em homem de 35 anos.

Tumor of the follicular infundibulum is an uncommon cutaneous lesion with different forms of clinical presentation, namely solitary and multiple/eruptive variants. The former shows predilection for head and neck and presents as a papulonodular scaly tumor. The latter is less frequent and occurs on facial, neck and upper chest areas as brown, reddish or more commonly hypopigmented macules leading to the differential diagnosis with vitiligo. The different clinical forms share the same histopathologic aspect. The present report describes a case of the multiple variant of tumor of the follicular infundibulum disclosing facial vitiligoid macules in a 35-year-old male patient.

Infecções parasitárias do apêndice cecal e suas relações com apendicite aguda / Parasitic infection of the appendix and its possible relationship to acute appendicitis

Investigou-se a prevalência de infecções parasitárias do apêndice cecal e suas relações com a apendicite. Dos 1.600 apêndices estudados 24 (1,5 por cento) apresentaram infecção parasitária. Enterobius vermicularis foi encontrado em 23 casos (95,8 por cento) e Taenia sp em apenas um (4,2 por cento). Dezesseis pacientes (66,7 por cento) eram menores de 10 anos; 15 eram masculinos e 9 femininos. A análise histopatológica demonstrou inflamação aguda supurativa em 12 casos (50 por cento), eosinofilia em 13 (54,2 por cento) e hiperplasia linfóide em 10 (41,7 por cento). Complicações como peritonite ocorreram em 11 e gangrena em 3 casos. As infecções parasitárias do apêndice são causa pouco freqüente de apendicite aguda em crianças e adolescentes.

From 1,600 surgically removed appendices, 24 (1.5 percent) were found to have helminths. Enterobius vermicularis was observed in 23 of the 24 specimens (95.8 percent) and Taenia sp was detected in only 1 (4.2 percent) case. Sixteen patients (66.7 percent) were less than 10 year-old; 15 patients were male and 9 female. Pathologic analysis disclosed acute neutrophilic inflammation in 12 cases and lymphoid hyperplasia in 10 of the 24 appendices. Gangrenous appendicitis was diagnosed in 3 cases and peritonitis was found in 11 of the 24 infested appendices. Parasitic infection of the appendix is an uncommon cause of acute appendicitis in children and adolescents.